TWI436769B - 類Ｐｏｌｏ激酶抑制劑 - Google Patents

類Ｐｏｌｏ激酶抑制劑 Download PDF

Info

Publication number: TWI436769B
Authority: TW; Taiwan
Prior art keywords: alkyl; group; hetero; methyl; tetrahydro
Prior art date: 2007-09-25

Application number

TW097137049A

Other languages

English (en)

Chinese (zh)

Other versions

TW200927135A (en

Inventor

Sheldon X Cao

Victoria Feher

Takashi Ichikawa

Benjamin Jones

Stephen W Kaldor

Andre A Kiryanov

Betty Lam

Yan Liu

Christopher Mcbride

Srinivasa Reddy Natala

Zhe Nie

Jeffrey A Stafford

Original Assignee

Takeda Pharmaceutical

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

2007-09-25

Filing date

2008-09-25

Publication date

2014-05-11

Family has litigation

First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=40219644&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=TWI436769(B) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.

2008-09-25 Application filed by Takeda Pharmaceutical filed Critical Takeda Pharmaceutical

2009-07-01 Publication of TW200927135A publication Critical patent/TW200927135A/zh

2014-05-11 Application granted granted Critical

2014-05-11 Publication of TWI436769B publication Critical patent/TWI436769B/zh

Links

239000002770 polo like kinase inhibitor Substances 0.000 title description 2
125000000217 alkyl group Chemical group 0.000 claims description 1075
125000005842 heteroatom Chemical group 0.000 claims description 885
125000003118 aryl group Chemical group 0.000 claims description 565
125000000753 cycloalkyl group Chemical group 0.000 claims description 546
125000000008 (C1-C10) alkyl group Chemical group 0.000 claims description 400
-1 cyano, thio, oxy, hydroxy, carbonyloxy Chemical group 0.000 claims description 357
150000001602 bicycloalkyls Chemical group 0.000 claims description 272
125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims description 198
125000005843 halogen group Chemical group 0.000 claims description 186
229910052739 hydrogen Inorganic materials 0.000 claims description 179
239000001257 hydrogen Substances 0.000 claims description 179
125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 claims description 160
125000000475 sulfinyl group Chemical group [*:2]S([*:1])=O 0.000 claims description 156
125000002619 bicyclic group Chemical group 0.000 claims description 143
125000004435 hydrogen atom Chemical class [H]* 0.000 claims description 121
150000001875 compounds Chemical class 0.000 claims description 108
125000001072 heteroaryl group Chemical group 0.000 claims description 103
125000004104 aryloxy group Chemical group 0.000 claims description 100
125000005740 oxycarbonyl group Chemical group [*:1]OC([*:2])=O 0.000 claims description 97
125000002813 thiocarbonyl group Chemical group *C(*)=S 0.000 claims description 88
125000001424 substituent group Chemical group 0.000 claims description 87
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 85
125000003282 alkyl amino group Chemical group 0.000 claims description 70
125000001841 imino group Chemical group [H]N=* 0.000 claims description 69
125000003545 alkoxy group Chemical group 0.000 claims description 68
KXDAEFPNCMNJSK-UHFFFAOYSA-N benzene carboxamide Natural products NC(=O)C1=CC=CC=C1 KXDAEFPNCMNJSK-UHFFFAOYSA-N 0.000 claims description 66
125000005553 heteroaryloxy group Chemical group 0.000 claims description 57
150000003839 salts Chemical class 0.000 claims description 57
QQEWMMRFXYVLQU-UHFFFAOYSA-N decylhydrazine Chemical compound CCCCCCCCCCNN QQEWMMRFXYVLQU-UHFFFAOYSA-N 0.000 claims description 55
125000006296 sulfonyl amino group Chemical group [H]N(*)S(*)(=O)=O 0.000 claims description 36
150000001335 aliphatic alkanes Chemical class 0.000 claims description 33
125000004397 aminosulfonyl group Chemical group NS(=O)(=O)* 0.000 claims description 31
125000000027 (C1-C10) alkoxy group Chemical group 0.000 claims description 22
125000003342 alkenyl group Chemical group 0.000 claims description 22
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 claims description 18
229910052736 halogen Inorganic materials 0.000 claims description 14
239000003814 drug Substances 0.000 claims description 7
125000001153 fluoro group Chemical group F* 0.000 claims description 7
239000000470 constituent Substances 0.000 claims description 6
239000008194 pharmaceutical composition Substances 0.000 claims description 6
IHWDSEPNZDYMNF-UHFFFAOYSA-N 1H-indol-2-amine Chemical compound C1=CC=C2NC(N)=CC2=C1 IHWDSEPNZDYMNF-UHFFFAOYSA-N 0.000 claims description 5
FGRHPASIBCUARJ-UHFFFAOYSA-N 4-[(9-cyclohexyl-7,7-difluoro-5-methyl-6-oxo-8h-pyrimido[4,5-b][1,4]diazepin-2-yl)amino]-3-methoxy-n-(1-methylpiperidin-4-yl)benzamide Chemical compound COC1=CC(C(=O)NC2CCN(C)CC2)=CC=C1NC(N=C12)=NC=C1N(C)C(=O)C(F)(F)CN2C1CCCCC1 FGRHPASIBCUARJ-UHFFFAOYSA-N 0.000 claims description 3
125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 claims description 3
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 3
RMRKQITUAKRBEC-UHFFFAOYSA-N 4-[(9-cyclohexyl-7,7-difluoro-5-methyl-6-oxo-8h-pyrimido[4,5-b][1,4]diazepin-2-yl)amino]-3-methoxy-n-(8-methyl-8-azabicyclo[3.2.1]octan-3-yl)benzamide Chemical compound COC1=CC(C(=O)NC2CC3CCC(N3C)C2)=CC=C1NC(N=C12)=NC=C1N(C)C(=O)C(F)(F)CN2C1CCCCC1 RMRKQITUAKRBEC-UHFFFAOYSA-N 0.000 claims description 2
JIWASSBNCQACGB-KRWDZBQOSA-N 4-[(9-cyclohexyl-7,7-difluoro-5-methyl-6-oxo-8h-pyrimido[4,5-b][1,4]diazepin-2-yl)amino]-3-methoxy-n-[(3s)-pyrrolidin-3-yl]benzamide Chemical compound COC1=CC(C(=O)N[C@@H]2CNCC2)=CC=C1NC(N=C12)=NC=C1N(C)C(=O)C(F)(F)CN2C1CCCCC1 JIWASSBNCQACGB-KRWDZBQOSA-N 0.000 claims description 2
HRGFYVLLNOAVFY-UHFFFAOYSA-N 4-[(9-cyclohexyl-7,7-difluoro-5-methyl-6-oxo-8h-pyrimido[4,5-b][1,4]diazepin-2-yl)amino]-n-(1-ethylpiperidin-4-yl)-3-methoxybenzamide Chemical compound C1CN(CC)CCC1NC(=O)C(C=C1OC)=CC=C1NC1=NC=C(N(C)C(=O)C(F)(F)CN2C3CCCCC3)C2=N1 HRGFYVLLNOAVFY-UHFFFAOYSA-N 0.000 claims description 2
BQPHHOYAKRDPEI-DENIHFKCSA-N 4-[(9-cyclohexyl-7,7-difluoro-5-methyl-6-oxo-8h-pyrimido[4,5-b][1,4]diazepin-2-yl)amino]-n-[(1r,2r)-2-hydroxycyclohexyl]-3-methoxybenzamide Chemical compound COC1=CC(C(=O)N[C@H]2[C@@H](CCCC2)O)=CC=C1NC(N=C12)=NC=C1N(C)C(=O)C(F)(F)CN2C1CCCCC1 BQPHHOYAKRDPEI-DENIHFKCSA-N 0.000 claims description 2
OZTBNNQBOHWSGL-UHFFFAOYSA-N 4-[(9-cyclopentyl-7,7-difluoro-5-methyl-6-oxo-8h-pyrimido[4,5-b][1,4]diazepin-2-yl)amino]-n-cyclopropyl-3-methoxybenzamide Chemical compound COC1=CC(C(=O)NC2CC2)=CC=C1NC(N=C12)=NC=C1N(C)C(=O)C(F)(F)CN2C1CCCC1 OZTBNNQBOHWSGL-UHFFFAOYSA-N 0.000 claims description 2
RBXLZSWSJTUVKC-UHFFFAOYSA-N 4-[(9-cyclopentyl-7-ethenyl-7-fluoro-5-methyl-6-oxo-8h-pyrimido[4,5-b][1,4]diazepin-2-yl)amino]-3-methoxy-n-(1-methylpiperidin-4-yl)benzamide Chemical compound COC1=CC(C(=O)NC2CCN(C)CC2)=CC=C1NC(N=C12)=NC=C1N(C)C(=O)C(F)(C=C)CN2C1CCCC1 RBXLZSWSJTUVKC-UHFFFAOYSA-N 0.000 claims description 2
QEIJYXMTALGXJH-LJAQVGFWSA-N 4-[[(7s)-9-cyclopentyl-7-ethyl-7-fluoro-5-methyl-6-oxo-8h-pyrimido[4,5-b][1,4]diazepin-2-yl]amino]-3-methoxy-n-(1-methylpiperidin-4-yl)benzamide Chemical compound C([C@@](C(N(C)C1=CN=C(NC=2C(=CC(=CC=2)C(=O)NC2CCN(C)CC2)OC)N=C11)=O)(F)CC)N1C1CCCC1 QEIJYXMTALGXJH-LJAQVGFWSA-N 0.000 claims description 2
125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 claims description 2
125000004356 hydroxy functional group Chemical group O* 0.000 claims 3
LRBDNFHJIHCMPR-LLVKDONJSA-N 3-methoxy-n-[(3r)-piperidin-3-yl]benzamide Chemical compound COC1=CC=CC(C(=O)N[C@H]2CNCCC2)=C1 LRBDNFHJIHCMPR-LLVKDONJSA-N 0.000 claims 1
SUPNECRXMVETSH-UHFFFAOYSA-N 4-[(9-cyclohexyl-7,7-difluoro-5-methyl-6-oxo-8h-pyrimido[4,5-b][1,4]diazepin-2-yl)amino]-3-methoxy-n-piperidin-4-ylbenzamide Chemical compound COC1=CC(C(=O)NC2CCNCC2)=CC=C1NC(N=C12)=NC=C1N(C)C(=O)C(F)(F)CN2C1CCCCC1 SUPNECRXMVETSH-UHFFFAOYSA-N 0.000 claims 1
QEVXKTASXHHSBC-UHFFFAOYSA-N 4-[(9-cyclohexyl-7,7-difluoro-5-methyl-6-oxo-8h-pyrimido[4,5-b][1,4]diazepin-2-yl)amino]-n-cyclopropyl-3-methoxybenzamide Chemical compound COC1=CC(C(=O)NC2CC2)=CC=C1NC(N=C12)=NC=C1N(C)C(=O)C(F)(F)CN2C1CCCCC1 QEVXKTASXHHSBC-UHFFFAOYSA-N 0.000 claims 1
RXDSAQWDJRAMCT-UHFFFAOYSA-N 4-[(9-cyclopentyl-7,7-difluoro-5-methyl-6-oxo-8h-pyrimido[4,5-b][1,4]diazepin-2-yl)amino]-2-fluoro-3-methoxy-n-(1-methylpiperidin-4-yl)benzamide Chemical compound C1=CC(C(=O)NC2CCN(C)CC2)=C(F)C(OC)=C1NC(N=C12)=NC=C1N(C)C(=O)C(F)(F)CN2C1CCCC1 RXDSAQWDJRAMCT-UHFFFAOYSA-N 0.000 claims 1
XOZMFYOPLYFBHK-UHFFFAOYSA-N 4-[(9-cyclopentyl-7,7-difluoro-5-methyl-6-oxo-8h-pyrimido[4,5-b][1,4]diazepin-2-yl)amino]-2-fluoro-n-(1-methylpiperidin-4-yl)benzamide Chemical compound C1CN(C)CCC1NC(=O)C(C(=C1)F)=CC=C1NC1=NC=C(N(C)C(=O)C(F)(F)CN2C3CCCC3)C2=N1 XOZMFYOPLYFBHK-UHFFFAOYSA-N 0.000 claims 1
JMBATVPHKFZTAF-UHFFFAOYSA-N 4-[(9-cyclopentyl-7,7-difluoro-5-methyl-6-oxo-8h-pyrimido[4,5-b][1,4]diazepin-2-yl)amino]-2-methoxy-n-(1-methylpiperidin-4-yl)benzamide Chemical compound C=1C=C(C(=O)NC2CCN(C)CC2)C(OC)=CC=1NC(N=C12)=NC=C1N(C)C(=O)C(F)(F)CN2C1CCCC1 JMBATVPHKFZTAF-UHFFFAOYSA-N 0.000 claims 1
XCXUJMZIPNJQGW-UHFFFAOYSA-N 4-[(9-cyclopentyl-7,7-difluoro-5-methyl-6-oxo-8h-pyrimido[4,5-b][1,4]diazepin-2-yl)amino]-3-ethyl-n-(1-methylpiperidin-4-yl)benzamide Chemical compound CCC1=CC(C(=O)NC2CCN(C)CC2)=CC=C1NC(N=C12)=NC=C1N(C)C(=O)C(F)(F)CN2C1CCCC1 XCXUJMZIPNJQGW-UHFFFAOYSA-N 0.000 claims 1
QFLZTKMRVNTGQH-UHFFFAOYSA-N 4-[(9-cyclopentyl-7,7-difluoro-5-methyl-6-oxo-8h-pyrimido[4,5-b][1,4]diazepin-2-yl)amino]-n-(1-ethylpiperidin-4-yl)-3-methoxybenzamide Chemical compound C1CN(CC)CCC1NC(=O)C(C=C1OC)=CC=C1NC1=NC=C(N(C)C(=O)C(F)(F)CN2C3CCCC3)C2=N1 QFLZTKMRVNTGQH-UHFFFAOYSA-N 0.000 claims 1
QEIJYXMTALGXJH-UHFFFAOYSA-N 4-[(9-cyclopentyl-7-ethyl-7-fluoro-5-methyl-6-oxo-8h-pyrimido[4,5-b][1,4]diazepin-2-yl)amino]-3-methoxy-n-(1-methylpiperidin-4-yl)benzamide Chemical compound C12=NC(NC=3C(=CC(=CC=3)C(=O)NC3CCN(C)CC3)OC)=NC=C2N(C)C(=O)C(CC)(F)CN1C1CCCC1 QEIJYXMTALGXJH-UHFFFAOYSA-N 0.000 claims 1
JYAPSFXNGNGAEG-GDLZYMKVSA-N 4-[[(7r)-9-cyclopentyl-7-ethenyl-7-fluoro-5-methyl-6-oxo-8h-pyrimido[4,5-b][1,4]diazepin-2-yl]amino]-2-fluoro-5-methoxy-n-(1-methylpiperidin-4-yl)benzamide Chemical compound FC=1C=C(NC=2N=C3N(C4CCCC4)C[C@@](F)(C(=O)N(C)C3=CN=2)C=C)C(OC)=CC=1C(=O)NC1CCN(C)CC1 JYAPSFXNGNGAEG-GDLZYMKVSA-N 0.000 claims 1
RBXLZSWSJTUVKC-GDLZYMKVSA-N 4-[[(7r)-9-cyclopentyl-7-ethenyl-7-fluoro-5-methyl-6-oxo-8h-pyrimido[4,5-b][1,4]diazepin-2-yl]amino]-3-methoxy-n-(1-methylpiperidin-4-yl)benzamide Chemical compound C([C@@](F)(C(=O)N(C)C1=CN=C(N=C11)NC2=CC=C(C=C2OC)C(=O)NC2CCN(C)CC2)C=C)N1C1CCCC1 RBXLZSWSJTUVKC-GDLZYMKVSA-N 0.000 claims 1
JGKRKGWWOJGNBQ-WHLCRQNOSA-N 4-[[(7r)-9-cyclopentyl-7-ethenyl-7-fluoro-5-methyl-6-oxo-8h-pyrimido[4,5-b][1,4]diazepin-2-yl]amino]-3-methoxy-n-[(3r)-piperidin-3-yl]benzamide Chemical compound C([C@@](F)(C(=O)N(C)C1=CN=C(N=C11)NC2=CC=C(C=C2OC)C(=O)N[C@H]2CNCCC2)C=C)N1C1CCCC1 JGKRKGWWOJGNBQ-WHLCRQNOSA-N 0.000 claims 1
GYTNYDFGRYCVLH-SSEXGKCCSA-N 4-[[(7r)-9-cyclopentyl-7-ethenyl-7-fluoro-5-methyl-6-oxo-8h-pyrimido[4,5-b][1,4]diazepin-2-yl]amino]-n-(1-ethylpiperidin-4-yl)-3-methoxybenzamide Chemical compound C1CN(CC)CCC1NC(=O)C(C=C1OC)=CC=C1NC1=NC=C(N(C)C(=O)[C@](F)(CN2C3CCCC3)C=C)C2=N1 GYTNYDFGRYCVLH-SSEXGKCCSA-N 0.000 claims 1
RWCCWEUUXYIKHB-UHFFFAOYSA-N benzophenone Chemical compound C=1C=CC=CC=1C(=O)C1=CC=CC=C1 RWCCWEUUXYIKHB-UHFFFAOYSA-N 0.000 claims 1
239000012965 benzophenone Substances 0.000 claims 1
125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims 1
125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims 1
NFHFRUOZVGFOOS-UHFFFAOYSA-N palladium;triphenylphosphane Chemical compound [Pd].C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 NFHFRUOZVGFOOS-UHFFFAOYSA-N 0.000 claims 1
239000000546 pharmaceutical excipient Substances 0.000 claims 1
ROSDSFDQCJNGOL-UHFFFAOYSA-N protonated dimethyl amine Natural products CNC ROSDSFDQCJNGOL-UHFFFAOYSA-N 0.000 claims 1
IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 71
125000002887 hydroxy group Chemical group [H]O* 0.000 description 69
239000003112 inhibitor Substances 0.000 description 66
101000582926 Dictyostelium discoideum Probable serine/threonine-protein kinase PLK Proteins 0.000 description 65
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 62
229910052757 nitrogen Inorganic materials 0.000 description 55
229910052799 carbon Inorganic materials 0.000 description 45
208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 43
125000004429 atom Chemical group 0.000 description 40
238000000034 method Methods 0.000 description 39
201000010099 disease Diseases 0.000 description 38
XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 36
239000007795 chemical reaction product Substances 0.000 description 36
108091000080 Phosphotransferase Proteins 0.000 description 32
102000020233 phosphotransferase Human genes 0.000 description 32
229910052717 sulfur Chemical group 0.000 description 32
229910052760 oxygen Inorganic materials 0.000 description 30
239000000203 mixture Substances 0.000 description 28
125000003277 amino group Chemical group 0.000 description 27
125000004093 cyano group Chemical group *C#N 0.000 description 26
238000001727 in vivo Methods 0.000 description 26
125000000229 (C1-C4)alkoxy group Chemical group 0.000 description 25
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 25
239000002585 base Substances 0.000 description 25
HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 20
102000001253 Protein Kinase Human genes 0.000 description 20
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 20
108060006633 protein kinase Proteins 0.000 description 20
150000001412 amines Chemical class 0.000 description 19
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 19
125000002947 alkylene group Chemical group 0.000 description 18
125000004432 carbon atom Chemical group C* 0.000 description 18
229940124530 sulfonamide Drugs 0.000 description 18
150000003456 sulfonamides Chemical class 0.000 description 18
125000000304 alkynyl group Chemical group 0.000 description 16
125000004178 (C1-C4) alkyl group Chemical group 0.000 description 15
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 15
125000006652 (C3-C12) cycloalkyl group Chemical group 0.000 description 14
238000004519 manufacturing process Methods 0.000 description 14
125000001820 oxy group Chemical group [*:1]O[*:2] 0.000 description 14
239000001301 oxygen Chemical group 0.000 description 14
125000000592 heterocycloalkyl group Chemical group 0.000 description 13
125000005647 linker group Chemical group 0.000 description 13
206010028980 Neoplasm Diseases 0.000 description 12
210000004027 cell Anatomy 0.000 description 12
150000002148 esters Chemical class 0.000 description 12
125000000468 ketone group Chemical group 0.000 description 12
239000011593 sulfur Chemical group 0.000 description 12
NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 11
150000001721 carbon Chemical group 0.000 description 11
230000000694 effects Effects 0.000 description 11
125000005429 oxyalkyl group Chemical group 0.000 description 11
PXQLVRUNWNTZOS-UHFFFAOYSA-N sulfanyl Chemical compound [SH] PXQLVRUNWNTZOS-UHFFFAOYSA-N 0.000 description 11
150000002466 imines Chemical class 0.000 description 10
230000007170 pathology Effects 0.000 description 10
241000282414 Homo sapiens Species 0.000 description 9
150000002367 halogens Chemical class 0.000 description 9
125000000879 imine group Chemical group 0.000 description 9
230000002401 inhibitory effect Effects 0.000 description 9
108090000765 processed proteins & peptides Chemical group 0.000 description 9
108090000623 proteins and genes Proteins 0.000 description 9
125000006413 ring segment Chemical group 0.000 description 9
229920006395 saturated elastomer Polymers 0.000 description 9
BUUPQKDIAURBJP-UHFFFAOYSA-N sulfinic acid Chemical compound OS=O BUUPQKDIAURBJP-UHFFFAOYSA-N 0.000 description 9
125000003396 thiol group Chemical group [H]S* 0.000 description 9
238000011282 treatment Methods 0.000 description 9
102000004190 Enzymes Human genes 0.000 description 8
108090000790 Enzymes Proteins 0.000 description 8
OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 description 8
NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 8
JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 8
239000002253 acid Substances 0.000 description 8
125000001118 alkylidene group Chemical group 0.000 description 8
125000000539 amino acid group Chemical group 0.000 description 8
125000004112 carboxyamino group Chemical group [H]OC(=O)N([H])[*] 0.000 description 8
238000006243 chemical reaction Methods 0.000 description 8
125000006239 protecting group Chemical group 0.000 description 8
102000004169 proteins and genes Human genes 0.000 description 8
229930194542 Keto Natural products 0.000 description 7
241001465754 Metazoa Species 0.000 description 7
201000011510 cancer Diseases 0.000 description 7
229940002612 prodrug Drugs 0.000 description 7
239000000651 prodrug Substances 0.000 description 7
208000024891 symptom Diseases 0.000 description 7
210000003708 urethra Anatomy 0.000 description 7
125000002252 acyl group Chemical group 0.000 description 6
125000001931 aliphatic group Chemical group 0.000 description 6
MWPLVEDNUUSJAV-UHFFFAOYSA-N anthracene Chemical compound C1=CC=CC2=CC3=CC=CC=C3C=C21 MWPLVEDNUUSJAV-UHFFFAOYSA-N 0.000 description 6
WGQKYBSKWIADBV-UHFFFAOYSA-N benzylamine Chemical compound NCC1=CC=CC=C1 WGQKYBSKWIADBV-UHFFFAOYSA-N 0.000 description 6
QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 6
208000011580 syndromic disease Diseases 0.000 description 6
108700020796 Oncogene Proteins 0.000 description 5
201000004681 Psoriasis Diseases 0.000 description 5
125000002723 alicyclic group Chemical group 0.000 description 5
150000001413 amino acids Chemical class 0.000 description 5
125000001584 benzyloxycarbonyl group Chemical group C(=O)(OCC1=CC=CC=C1)* 0.000 description 5
125000005708 carbonyloxy group Chemical group [*:2]OC([*:1])=O 0.000 description 5
125000001309 chloro group Chemical group Cl* 0.000 description 5
208000035475 disorder Diseases 0.000 description 5
125000000623 heterocyclic group Chemical group 0.000 description 5
230000005764 inhibitory process Effects 0.000 description 5
229940043355 kinase inhibitor Drugs 0.000 description 5
125000002950 monocyclic group Chemical group 0.000 description 5
UYWQUFXKFGHYNT-UHFFFAOYSA-N phenylmethyl ester of formic acid Natural products O=COCC1=CC=CC=C1 UYWQUFXKFGHYNT-UHFFFAOYSA-N 0.000 description 5
239000003757 phosphotransferase inhibitor Substances 0.000 description 5
125000003367 polycyclic group Chemical group 0.000 description 5
125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 5
235000018102 proteins Nutrition 0.000 description 5
BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 5
YROXIXLRRCOBKF-UHFFFAOYSA-N sulfonylurea Chemical group OC(=N)N=S(=O)=O YROXIXLRRCOBKF-UHFFFAOYSA-N 0.000 description 5
YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 5
GVNVAWHJIKLAGL-UHFFFAOYSA-N 2-(cyclohexen-1-yl)cyclohexan-1-one Chemical compound O=C1CCCCC1C1=CCCCC1 GVNVAWHJIKLAGL-UHFFFAOYSA-N 0.000 description 4
201000004384 Alopecia Diseases 0.000 description 4
208000024827 Alzheimer disease Diseases 0.000 description 4
101150065749 Churc1 gene Proteins 0.000 description 4
RGSFGYAAUTVSQA-UHFFFAOYSA-N Cyclopentane Chemical compound C1CCCC1 RGSFGYAAUTVSQA-UHFFFAOYSA-N 0.000 description 4
MHZGKXUYDGKKIU-UHFFFAOYSA-N Decylamine Chemical compound CCCCCCCCCCN MHZGKXUYDGKKIU-UHFFFAOYSA-N 0.000 description 4
FFEARJCKVFRZRR-BYPYZUCNSA-N L-methionine Chemical compound CSCC[C@H](N)C(O)=O FFEARJCKVFRZRR-BYPYZUCNSA-N 0.000 description 4
AYFVYJQAPQTCCC-GBXIJSLDSA-N L-threonine Chemical compound C[C@@H](O)[C@H](N)C(O)=O AYFVYJQAPQTCCC-GBXIJSLDSA-N 0.000 description 4
102100038239 Protein Churchill Human genes 0.000 description 4
RWRDLPDLKQPQOW-UHFFFAOYSA-N Pyrrolidine Chemical compound C1CCNC1 RWRDLPDLKQPQOW-UHFFFAOYSA-N 0.000 description 4
SMWDFEZZVXVKRB-UHFFFAOYSA-N Quinoline Chemical compound N1=CC=CC2=CC=CC=C21 SMWDFEZZVXVKRB-UHFFFAOYSA-N 0.000 description 4
DZBUGLKDJFMEHC-UHFFFAOYSA-N acridine Chemical compound C1=CC=CC2=CC3=CC=CC=C3N=C21 DZBUGLKDJFMEHC-UHFFFAOYSA-N 0.000 description 4
150000001299 aldehydes Chemical class 0.000 description 4
229910000147 aluminium phosphate Inorganic materials 0.000 description 4
235000001014 amino acid Nutrition 0.000 description 4
229940024606 amino acid Drugs 0.000 description 4
150000001540 azides Chemical class 0.000 description 4
239000011203 carbon fibre reinforced carbon Substances 0.000 description 4
230000022131 cell cycle Effects 0.000 description 4
125000004122 cyclic group Chemical group 0.000 description 4
239000000543 intermediate Substances 0.000 description 4
150000002576 ketones Chemical class 0.000 description 4
150000002632 lipids Chemical class 0.000 description 4
229930182817 methionine Natural products 0.000 description 4
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 4
201000008383 nephritis Diseases 0.000 description 4
239000005022 packaging material Substances 0.000 description 4
UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 4
238000000926 separation method Methods 0.000 description 4
125000005415 substituted alkoxy group Chemical group 0.000 description 4
125000004434 sulfur atom Chemical group 0.000 description 4
238000002560 therapeutic procedure Methods 0.000 description 4
125000004149 thio group Chemical group *S* 0.000 description 4
125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 4
MTCFGRXMJLQNBG-REOHCLBHSA-N (2S)-2-Amino-3-hydroxypropansäure Chemical compound OC[C@H](N)C(O)=O MTCFGRXMJLQNBG-REOHCLBHSA-N 0.000 description 3
MNWSGMTUGXNYHJ-UHFFFAOYSA-N 2-methoxybenzamide Chemical compound COC1=CC=CC=C1C(N)=O MNWSGMTUGXNYHJ-UHFFFAOYSA-N 0.000 description 3
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
208000024172 Cardiovascular disease Diseases 0.000 description 3
WHUUTDBJXJRKMK-UHFFFAOYSA-N Glutamic acid Natural products OC(=O)C(N)CCC(O)=O WHUUTDBJXJRKMK-UHFFFAOYSA-N 0.000 description 3
DHMQDGOQFOQNFH-UHFFFAOYSA-N Glycine Chemical compound NCC(O)=O DHMQDGOQFOQNFH-UHFFFAOYSA-N 0.000 description 3
CKLJMWTZIZZHCS-REOHCLBHSA-N L-aspartic acid Chemical compound OC(=O)[C@@H](N)CC(O)=O CKLJMWTZIZZHCS-REOHCLBHSA-N 0.000 description 3
WHUUTDBJXJRKMK-VKHMYHEASA-N L-glutamic acid Chemical compound OC(=O)[C@@H](N)CCC(O)=O WHUUTDBJXJRKMK-VKHMYHEASA-N 0.000 description 3
ROHFNLRQFUQHCH-YFKPBYRVSA-N L-leucine Chemical compound CC(C)C[C@H](N)C(O)=O ROHFNLRQFUQHCH-YFKPBYRVSA-N 0.000 description 3
COLNVLDHVKWLRT-QMMMGPOBSA-N L-phenylalanine Chemical compound OC(=O)[C@@H](N)CC1=CC=CC=C1 COLNVLDHVKWLRT-QMMMGPOBSA-N 0.000 description 3
OUYCCCASQSFEME-QMMMGPOBSA-N L-tyrosine Chemical compound OC(=O)[C@@H](N)CC1=CC=C(O)C=C1 OUYCCCASQSFEME-QMMMGPOBSA-N 0.000 description 3
108091054455 MAP kinase family Proteins 0.000 description 3
102000043136 MAP kinase family Human genes 0.000 description 3
OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 3
KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
WTKZEGDFNFYCGP-UHFFFAOYSA-N Pyrazole Chemical compound C=1C=NNC=1 WTKZEGDFNFYCGP-UHFFFAOYSA-N 0.000 description 3
CZPWVGJYEJSRLH-UHFFFAOYSA-N Pyrimidine Chemical compound C1=CN=CN=C1 CZPWVGJYEJSRLH-UHFFFAOYSA-N 0.000 description 3
102100031463 Serine/threonine-protein kinase PLK1 Human genes 0.000 description 3
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
HSFWRNGVRCDJHI-UHFFFAOYSA-N alpha-acetylene Natural products C#C HSFWRNGVRCDJHI-UHFFFAOYSA-N 0.000 description 3
125000005101 aryl methoxy carbonyl group Chemical group 0.000 description 3
WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 3
125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 3
125000003739 carbamimidoyl group Chemical group C(N)(=N)* 0.000 description 3
125000001951 carbamoylamino group Chemical group C(N)(=O)N* 0.000 description 3
210000003169 central nervous system Anatomy 0.000 description 3
KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 3
229940079593 drug Drugs 0.000 description 3
125000002534 ethynyl group Chemical group [H]C#C* 0.000 description 3
ZHNUHDYFZUAESO-UHFFFAOYSA-N formamide Substances NC=O ZHNUHDYFZUAESO-UHFFFAOYSA-N 0.000 description 3
DMEGYFMYUHOHGS-UHFFFAOYSA-N heptamethylene Natural products C1CCCCCC1 DMEGYFMYUHOHGS-UHFFFAOYSA-N 0.000 description 3
125000004404 heteroalkyl group Chemical group 0.000 description 3
UKAUYVFTDYCKQA-UHFFFAOYSA-N homoserine Chemical compound OC(=O)C(N)CCO UKAUYVFTDYCKQA-UHFFFAOYSA-N 0.000 description 3
NOVHEGOWZNFVGT-UHFFFAOYSA-N hydrazine Chemical compound NN.NN NOVHEGOWZNFVGT-UHFFFAOYSA-N 0.000 description 3
230000007062 hydrolysis Effects 0.000 description 3
238000006460 hydrolysis reaction Methods 0.000 description 3
RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Natural products C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 description 3
SUMDYPCJJOFFON-UHFFFAOYSA-N isethionic acid Chemical compound OCCS(O)(=O)=O SUMDYPCJJOFFON-UHFFFAOYSA-N 0.000 description 3
230000001404 mediated effect Effects 0.000 description 3
125000001434 methanylylidene group Chemical group [H]C#[*] 0.000 description 3
VMGAPWLDMVPYIA-HIDZBRGKSA-N n'-amino-n-iminomethanimidamide Chemical group N\N=C\N=N VMGAPWLDMVPYIA-HIDZBRGKSA-N 0.000 description 3
125000004433 nitrogen atom Chemical group N* 0.000 description 3
125000004430 oxygen atom Chemical group O* 0.000 description 3
108010056274 polo-like kinase 1 Proteins 0.000 description 3
230000008569 process Effects 0.000 description 3
230000002062 proliferating effect Effects 0.000 description 3
125000004076 pyridyl group Chemical group 0.000 description 3
230000002829 reductive effect Effects 0.000 description 3
BOLDJAUMGUJJKM-LSDHHAIUSA-N renifolin D Natural products CC(=C)[C@@H]1Cc2c(O)c(O)ccc2[C@H]1CC(=O)c3ccc(O)cc3O BOLDJAUMGUJJKM-LSDHHAIUSA-N 0.000 description 3
208000037803 restenosis Diseases 0.000 description 3
230000019491 signal transduction Effects 0.000 description 3
239000012453 solvate Substances 0.000 description 3
238000003860 storage Methods 0.000 description 3
RWSOTUBLDIXVET-UHFFFAOYSA-O sulfonium group Chemical group [SH3+] RWSOTUBLDIXVET-UHFFFAOYSA-O 0.000 description 3
JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 3
VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 3
238000012546 transfer Methods 0.000 description 3
230000003612 virological effect Effects 0.000 description 3
125000003837 (C1-C20) alkyl group Chemical group 0.000 description 2
125000003161 (C1-C6) alkylene group Chemical group 0.000 description 2
VZXTWGWHSMCWGA-UHFFFAOYSA-N 1,3,5-triazine-2,4-diamine Chemical compound NC1=NC=NC(N)=N1 VZXTWGWHSMCWGA-UHFFFAOYSA-N 0.000 description 2
IANQTJSKSUMEQM-UHFFFAOYSA-N 1-benzofuran Chemical compound C1=CC=C2OC=CC2=C1 IANQTJSKSUMEQM-UHFFFAOYSA-N 0.000 description 2
FCEHBMOGCRZNNI-UHFFFAOYSA-N 1-benzothiophene Chemical compound C1=CC=C2SC=CC2=C1 FCEHBMOGCRZNNI-UHFFFAOYSA-N 0.000 description 2
125000006017 1-propenyl group Chemical group 0.000 description 2
MVXVYAKCVDQRLW-UHFFFAOYSA-N 1h-pyrrolo[2,3-b]pyridine Chemical compound C1=CN=C2NC=CC2=C1 MVXVYAKCVDQRLW-UHFFFAOYSA-N 0.000 description 2
WXTMDXOMEHJXQO-UHFFFAOYSA-N 2,5-dihydroxybenzoic acid Chemical compound OC(=O)C1=CC(O)=CC=C1O WXTMDXOMEHJXQO-UHFFFAOYSA-N 0.000 description 2
HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 2
SNDPXSYFESPGGJ-UHFFFAOYSA-N 2-aminopentanoic acid Chemical compound CCCC(N)C(O)=O SNDPXSYFESPGGJ-UHFFFAOYSA-N 0.000 description 2
125000004974 2-butenyl group Chemical group C(C=CC)* 0.000 description 2
125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 2
125000001494 2-propynyl group Chemical group [H]C#CC([H])([H])* 0.000 description 2
XMIIGOLPHOKFCH-UHFFFAOYSA-N 3-phenylpropionic acid Chemical compound OC(=O)CCC1=CC=CC=C1 XMIIGOLPHOKFCH-UHFFFAOYSA-N 0.000 description 2
SHBWZOHGEVPNGK-UHFFFAOYSA-N 4-[(9-cyclopentyl-7,7-difluoro-5-methyl-6-oxo-8h-pyrimido[4,5-b][1,4]diazepin-2-yl)amino]-3-methoxy-n-piperidin-4-ylbenzamide Chemical compound COC1=CC(C(=O)NC2CCNCC2)=CC=C1NC(N=C12)=NC=C1N(C)C(=O)C(F)(F)CN2C1CCCC1 SHBWZOHGEVPNGK-UHFFFAOYSA-N 0.000 description 2
125000000339 4-pyridyl group Chemical group N1=C([H])C([H])=C([*])C([H])=C1[H] 0.000 description 2
HVCNSAJVIFXBHU-UHFFFAOYSA-N 5-hydroxy-4-oxopentanoic acid Chemical compound OCC(=O)CCC(O)=O HVCNSAJVIFXBHU-UHFFFAOYSA-N 0.000 description 2
UJOBWOGCFQCDNV-UHFFFAOYSA-N 9H-carbazole Chemical compound C1=CC=C2C3=CC=CC=C3NC2=C1 UJOBWOGCFQCDNV-UHFFFAOYSA-N 0.000 description 2
208000030507 AIDS Diseases 0.000 description 2
241000233788 Arecaceae Species 0.000 description 2
206010003210 Arteriosclerosis Diseases 0.000 description 2
208000023275 Autoimmune disease Diseases 0.000 description 2
241000271566 Aves Species 0.000 description 2
239000005711 Benzoic acid Substances 0.000 description 2
208000020084 Bone disease Diseases 0.000 description 2
241000283690 Bos taurus Species 0.000 description 2
241000282472 Canis lupus familiaris Species 0.000 description 2
241000283707 Capra Species 0.000 description 2
241000282994 Cervidae Species 0.000 description 2
XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 2
RGHNJXZEOKUKBD-SQOUGZDYSA-N D-gluconic acid Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C(O)=O RGHNJXZEOKUKBD-SQOUGZDYSA-N 0.000 description 2
230000005778 DNA damage Effects 0.000 description 2
231100000277 DNA damage Toxicity 0.000 description 2
206010012289 Dementia Diseases 0.000 description 2
FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 description 2
241000283086 Equidae Species 0.000 description 2
208000000461 Esophageal Neoplasms Diseases 0.000 description 2
241000282326 Felis catus Species 0.000 description 2
VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 2
AEMRFAOFKBGASW-UHFFFAOYSA-N Glycolic acid Chemical compound OCC(O)=O AEMRFAOFKBGASW-UHFFFAOYSA-N 0.000 description 2
208000031886 HIV Infections Diseases 0.000 description 2
241000282412 Homo Species 0.000 description 2
208000023105 Huntington disease Diseases 0.000 description 2
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
206010020880 Hypertrophy Diseases 0.000 description 2
XQFRJNBWHJMXHO-RRKCRQDMSA-N IDUR Chemical compound C1[C@H](O)[C@@H](CO)O[C@H]1N1C(=O)NC(=O)C(I)=C1 XQFRJNBWHJMXHO-RRKCRQDMSA-N 0.000 description 2
SIKJAQJRHWYJAI-UHFFFAOYSA-N Indole Chemical compound C1=CC=C2NC=CC2=C1 SIKJAQJRHWYJAI-UHFFFAOYSA-N 0.000 description 2
HNDVDQJCIGZPNO-YFKPBYRVSA-N L-histidine Chemical compound OC(=O)[C@@H](N)CC1=CN=CN1 HNDVDQJCIGZPNO-YFKPBYRVSA-N 0.000 description 2
KDXKERNSBIXSRK-YFKPBYRVSA-N L-lysine Chemical compound NCCCC[C@H](N)C(O)=O KDXKERNSBIXSRK-YFKPBYRVSA-N 0.000 description 2
206010025323 Lymphomas Diseases 0.000 description 2
KDXKERNSBIXSRK-UHFFFAOYSA-N Lysine Natural products NCCCCC(N)C(O)=O KDXKERNSBIXSRK-UHFFFAOYSA-N 0.000 description 2
241000124008 Mammalia Species 0.000 description 2
AFVFQIVMOAPDHO-UHFFFAOYSA-N Methanesulfonic acid Chemical compound CS(O)(=O)=O AFVFQIVMOAPDHO-UHFFFAOYSA-N 0.000 description 2
206010028116 Mucosal inflammation Diseases 0.000 description 2
201000010927 Mucositis Diseases 0.000 description 2
UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 2
206010030155 Oesophageal carcinoma Diseases 0.000 description 2
241000283973 Oryctolagus cuniculus Species 0.000 description 2
ZCQWOFVYLHDMMC-UHFFFAOYSA-N Oxazole Chemical compound C1=COC=N1 ZCQWOFVYLHDMMC-UHFFFAOYSA-N 0.000 description 2
208000030852 Parasitic disease Diseases 0.000 description 2
208000031481 Pathologic Constriction Diseases 0.000 description 2
241001494479 Pecora Species 0.000 description 2
NQRYJNQNLNOLGT-UHFFFAOYSA-N Piperidine Chemical compound C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 description 2
ONIBWKKTOPOVIA-UHFFFAOYSA-N Proline Natural products OC(=O)C1CCCN1 ONIBWKKTOPOVIA-UHFFFAOYSA-N 0.000 description 2
KAESVJOAVNADME-UHFFFAOYSA-N Pyrrole Chemical compound C=1C=CNC=1 KAESVJOAVNADME-UHFFFAOYSA-N 0.000 description 2
LCTONWCANYUPML-UHFFFAOYSA-N Pyruvic acid Chemical compound CC(=O)C(O)=O LCTONWCANYUPML-UHFFFAOYSA-N 0.000 description 2
206010039491 Sarcoma Diseases 0.000 description 2
CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
241000282887 Suidae Species 0.000 description 2
QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
239000005864 Sulphur Substances 0.000 description 2
WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
YTPLMLYBLZKORZ-UHFFFAOYSA-N Thiophene Chemical compound C=1C=CSC=1 YTPLMLYBLZKORZ-UHFFFAOYSA-N 0.000 description 2
AYFVYJQAPQTCCC-UHFFFAOYSA-N Threonine Natural products CC(O)C(N)C(O)=O AYFVYJQAPQTCCC-UHFFFAOYSA-N 0.000 description 2
239000004473 Threonine Substances 0.000 description 2
102000004357 Transferases Human genes 0.000 description 2
108090000992 Transferases Proteins 0.000 description 2
KZSNJWFQEVHDMF-UHFFFAOYSA-N Valine Chemical compound CC(C)C(N)C(O)=O KZSNJWFQEVHDMF-UHFFFAOYSA-N 0.000 description 2
230000001154 acute effect Effects 0.000 description 2
238000007792 addition Methods 0.000 description 2
231100000360 alopecia Toxicity 0.000 description 2
206010002026 amyotrophic lateral sclerosis Diseases 0.000 description 2
150000004056 anthraquinones Chemical class 0.000 description 2
239000002246 antineoplastic agent Substances 0.000 description 2
230000006793 arrhythmia Effects 0.000 description 2
206010003119 arrhythmia Diseases 0.000 description 2
208000011775 arteriosclerosis disease Diseases 0.000 description 2
206010003246 arthritis Diseases 0.000 description 2
230000001580 bacterial effect Effects 0.000 description 2
SRSXLGNVWSONIS-UHFFFAOYSA-N benzenesulfonic acid Chemical compound OS(=O)(=O)C1=CC=CC=C1 SRSXLGNVWSONIS-UHFFFAOYSA-N 0.000 description 2
229940092714 benzenesulfonic acid Drugs 0.000 description 2
125000005605 benzo group Chemical group 0.000 description 2
235000010233 benzoic acid Nutrition 0.000 description 2
229960004365 benzoic acid Drugs 0.000 description 2
IOJUPLGTWVMSFF-UHFFFAOYSA-N benzothiazole Chemical compound C1=CC=C2SC=NC2=C1 IOJUPLGTWVMSFF-UHFFFAOYSA-N 0.000 description 2
239000008280 blood Substances 0.000 description 2
210000004556 brain Anatomy 0.000 description 2
125000002837 carbocyclic group Chemical group 0.000 description 2
230000003197 catalytic effect Effects 0.000 description 2
230000024245 cell differentiation Effects 0.000 description 2
230000001684 chronic effect Effects 0.000 description 2
206010009887 colitis Diseases 0.000 description 2
230000001276 controlling effect Effects 0.000 description 2
150000001924 cycloalkanes Chemical class 0.000 description 2
125000000392 cycloalkenyl group Chemical group 0.000 description 2
MGNZXYYWBUKAII-UHFFFAOYSA-N cyclohexa-1,3-diene Chemical compound C1CC=CC=C1 MGNZXYYWBUKAII-UHFFFAOYSA-N 0.000 description 2
HGCIXCUEYOPUTN-UHFFFAOYSA-N cyclohexene Chemical compound C1CCC=CC1 HGCIXCUEYOPUTN-UHFFFAOYSA-N 0.000 description 2
ZSWFCLXCOIISFI-UHFFFAOYSA-N cyclopentadiene Chemical compound C1C=CC=C1 ZSWFCLXCOIISFI-UHFFFAOYSA-N 0.000 description 2
LPIQUOYDBNQMRZ-UHFFFAOYSA-N cyclopentene Chemical compound C1CC=CC1 LPIQUOYDBNQMRZ-UHFFFAOYSA-N 0.000 description 2
229940127089 cytotoxic agent Drugs 0.000 description 2
NNBZCPXTIHJBJL-UHFFFAOYSA-N decalin Chemical compound C1CCCC2CCCCC21 NNBZCPXTIHJBJL-UHFFFAOYSA-N 0.000 description 2
GHVNFZFCNZKVNT-UHFFFAOYSA-N decanoic acid Chemical compound CCCCCCCCCC(O)=O GHVNFZFCNZKVNT-UHFFFAOYSA-N 0.000 description 2
238000011161 development Methods 0.000 description 2
230000018109 developmental process Effects 0.000 description 2
230000004069 differentiation Effects 0.000 description 2
NBIIXXVUZAFLBC-UHFFFAOYSA-M dihydrogenphosphate Chemical compound OP(O)([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-M 0.000 description 2
230000002255 enzymatic effect Effects 0.000 description 2
201000004101 esophageal cancer Diseases 0.000 description 2
CCIVGXIOQKPBKL-UHFFFAOYSA-M ethanesulfonate Chemical compound CCS([O-])(=O)=O CCIVGXIOQKPBKL-UHFFFAOYSA-M 0.000 description 2
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
229910052731 fluorine Inorganic materials 0.000 description 2
230000006870 function Effects 0.000 description 2
230000002538 fungal effect Effects 0.000 description 2
235000013922 glutamic acid Nutrition 0.000 description 2
239000004220 glutamic acid Substances 0.000 description 2
XKUKSGPZAADMRA-UHFFFAOYSA-N glycyl-glycyl-glycine Chemical compound NCC(=O)NCC(=O)NCC(O)=O XKUKSGPZAADMRA-UHFFFAOYSA-N 0.000 description 2
230000012010 growth Effects 0.000 description 2
210000004209 hair Anatomy 0.000 description 2
230000003676 hair loss Effects 0.000 description 2
MNWFXJYAOYHMED-UHFFFAOYSA-N heptanoic acid Chemical compound CCCCCCC(O)=O MNWFXJYAOYHMED-UHFFFAOYSA-N 0.000 description 2
125000006588 heterocycloalkylene group Chemical group 0.000 description 2
FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid Chemical compound CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 description 2
HNDVDQJCIGZPNO-UHFFFAOYSA-N histidine Natural products OC(=O)C(N)CC1=CN=CN1 HNDVDQJCIGZPNO-UHFFFAOYSA-N 0.000 description 2
150000002440 hydroxy compounds Chemical class 0.000 description 2
230000003463 hyperproliferative effect Effects 0.000 description 2
208000015181 infectious disease Diseases 0.000 description 2
208000027866 inflammatory disease Diseases 0.000 description 2
230000002757 inflammatory effect Effects 0.000 description 2
208000014674 injury Diseases 0.000 description 2
150000007529 inorganic bases Chemical class 0.000 description 2
210000000936 intestine Anatomy 0.000 description 2
125000000555 isopropenyl group Chemical group [H]\C([H])=C(\*)C([H])([H])[H] 0.000 description 2
AWJUIBRHMBBTKR-UHFFFAOYSA-N isoquinoline Chemical compound C1=NC=CC2=CC=CC=C21 AWJUIBRHMBBTKR-UHFFFAOYSA-N 0.000 description 2
JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 description 2
208000032839 leukemia Diseases 0.000 description 2
VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 2
230000007246 mechanism Effects 0.000 description 2
VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 2
125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 description 2
BQJCRHHNABKAKU-KBQPJGBKSA-N morphine Chemical compound O([C@H]1[C@H](C=C[C@H]23)O)C4=C5[C@@]12CCN(C)[C@@H]3CC5=CC=C4O BQJCRHHNABKAKU-KBQPJGBKSA-N 0.000 description 2
TXXHDPDFNKHHGW-UHFFFAOYSA-N muconic acid Chemical compound OC(=O)C=CC=CC(O)=O TXXHDPDFNKHHGW-UHFFFAOYSA-N 0.000 description 2
210000005036 nerve Anatomy 0.000 description 2
230000004770 neurodegeneration Effects 0.000 description 2
208000015122 neurodegenerative disease Diseases 0.000 description 2
208000002154 non-small cell lung carcinoma Diseases 0.000 description 2
150000007530 organic bases Chemical class 0.000 description 2
230000036961 partial effect Effects 0.000 description 2
238000010647 peptide synthesis reaction Methods 0.000 description 2
YNPNZTXNASCQKK-UHFFFAOYSA-N phenanthrene Chemical compound C1=CC=C2C3=CC=CC=C3C=CC2=C1 YNPNZTXNASCQKK-UHFFFAOYSA-N 0.000 description 2
XYFCBTPGUUZFHI-UHFFFAOYSA-O phosphonium Chemical compound [PH4+] XYFCBTPGUUZFHI-UHFFFAOYSA-O 0.000 description 2
125000005499 phosphonyl group Chemical group 0.000 description 2
230000026731 phosphorylation Effects 0.000 description 2
238000006366 phosphorylation reaction Methods 0.000 description 2
230000035755 proliferation Effects 0.000 description 2
230000009822 protein phosphorylation Effects 0.000 description 2
DVUBDHRTVYLIPA-UHFFFAOYSA-N pyrazolo[1,5-a]pyridine Chemical compound C1=CC=CN2N=CC=C21 DVUBDHRTVYLIPA-UHFFFAOYSA-N 0.000 description 2
125000004527 pyrimidin-4-yl group Chemical group N1=CN=C(C=C1)* 0.000 description 2
102000005962 receptors Human genes 0.000 description 2
108020003175 receptors Proteins 0.000 description 2
YGSDEFSMJLZEOE-UHFFFAOYSA-N salicylic acid Chemical compound OC(=O)C1=CC=CC=C1O YGSDEFSMJLZEOE-UHFFFAOYSA-N 0.000 description 2
208000017520 skin disease Diseases 0.000 description 2
125000003003 spiro group Chemical group 0.000 description 2
230000036262 stenosis Effects 0.000 description 2
208000037804 stenosis Diseases 0.000 description 2
239000000126 substance Substances 0.000 description 2
125000000020 sulfo group Chemical group O=S(=O)([*])O[H] 0.000 description 2
238000003786 synthesis reaction Methods 0.000 description 2
229940124597 therapeutic agent Drugs 0.000 description 2
125000004001 thioalkyl group Chemical group 0.000 description 2
230000008733 trauma Effects 0.000 description 2
125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 description 2
208000029729 tumor suppressor gene on chromosome 11 Diseases 0.000 description 2
230000029663 wound healing Effects 0.000 description 2
RRKODOZNUZCUBN-CCAGOZQPSA-N (1z,3z)-cycloocta-1,3-diene Chemical compound C1CC\C=C/C=C\C1 RRKODOZNUZCUBN-CCAGOZQPSA-N 0.000 description 1
AUXMWYRZQPIXCC-KNIFDHDWSA-N (2s)-2-amino-4-methylpentanoic acid;(2s)-2-aminopropanoic acid Chemical compound C[C@H](N)C(O)=O.CC(C)C[C@H](N)C(O)=O AUXMWYRZQPIXCC-KNIFDHDWSA-N 0.000 description 1
125000004169 (C1-C6) alkyl group Chemical group 0.000 description 1
MIOPJNTWMNEORI-GMSGAONNSA-N (S)-camphorsulfonic acid Chemical compound C1C[C@@]2(CS(O)(=O)=O)C(=O)C[C@@H]1C2(C)C MIOPJNTWMNEORI-GMSGAONNSA-N 0.000 description 1
BJEPYKJPYRNKOW-REOHCLBHSA-N (S)-malic acid Chemical compound OC(=O)[C@@H](O)CC(O)=O BJEPYKJPYRNKOW-REOHCLBHSA-N 0.000 description 1
WBYWAXJHAXSJNI-VOTSOKGWSA-M .beta-Phenylacrylic acid Natural products [O-]C(=O)\C=C\C1=CC=CC=C1 WBYWAXJHAXSJNI-VOTSOKGWSA-M 0.000 description 1
MBIZXFATKUQOOA-UHFFFAOYSA-N 1,3,4-thiadiazole Chemical compound C1=NN=CS1 MBIZXFATKUQOOA-UHFFFAOYSA-N 0.000 description 1
FTNJQNQLEGKTGD-UHFFFAOYSA-N 1,3-benzodioxole Chemical class C1=CC=C2OCOC2=C1 FTNJQNQLEGKTGD-UHFFFAOYSA-N 0.000 description 1
GWYPDXLJACEENP-UHFFFAOYSA-N 1,3-cycloheptadiene Chemical compound C1CC=CC=CC1 GWYPDXLJACEENP-UHFFFAOYSA-N 0.000 description 1
FLBAYUMRQUHISI-UHFFFAOYSA-N 1,8-naphthyridine Chemical compound N1=CC=CC2=CC=CN=C21 FLBAYUMRQUHISI-UHFFFAOYSA-N 0.000 description 1
GELASUFEZONUHG-UHFFFAOYSA-N 1-(sulfinylamino)decane Chemical compound CCCCCCCCCCN=S=O GELASUFEZONUHG-UHFFFAOYSA-N 0.000 description 1
125000004973 1-butenyl group Chemical group C(=CCC)* 0.000 description 1
KVDAFDJNVBMZDR-UHFFFAOYSA-N 1-hydroxydiaziridin-3-one Chemical compound ON1NC1=O KVDAFDJNVBMZDR-UHFFFAOYSA-N 0.000 description 1
AMMPLVWPWSYRDR-UHFFFAOYSA-N 1-methylbicyclo[2.2.2]oct-2-ene-4-carboxylic acid Chemical compound C1CC2(C(O)=O)CCC1(C)C=C2 AMMPLVWPWSYRDR-UHFFFAOYSA-N 0.000 description 1
125000004343 1-phenylethyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])(*)C([H])([H])[H] 0.000 description 1
125000000530 1-propynyl group Chemical group [H]C([H])([H])C#C* 0.000 description 1
HYZJCKYKOHLVJF-UHFFFAOYSA-N 1H-benzimidazole Chemical compound C1=CC=C2NC=NC2=C1 HYZJCKYKOHLVJF-UHFFFAOYSA-N 0.000 description 1
BAXOFTOLAUCFNW-UHFFFAOYSA-N 1H-indazole Chemical compound C1=CC=C2C=NNC2=C1 BAXOFTOLAUCFNW-UHFFFAOYSA-N 0.000 description 1
XLKDJOPOOHHZAN-UHFFFAOYSA-N 1h-pyrrolo[2,3-c]pyridine Chemical compound C1=NC=C2NC=CC2=C1 XLKDJOPOOHHZAN-UHFFFAOYSA-N 0.000 description 1
XWIYUCRMWCHYJR-UHFFFAOYSA-N 1h-pyrrolo[3,2-b]pyridine Chemical compound C1=CC=C2NC=CC2=N1 XWIYUCRMWCHYJR-UHFFFAOYSA-N 0.000 description 1
SRSKXJVMVSSSHB-UHFFFAOYSA-N 1h-pyrrolo[3,2-c]pyridine Chemical compound N1=CC=C2NC=CC2=C1 SRSKXJVMVSSSHB-UHFFFAOYSA-N 0.000 description 1
125000006029 2-methyl-2-butenyl group Chemical group 0.000 description 1
125000000094 2-phenylethyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])C([H])([H])* 0.000 description 1
125000006479 2-pyridyl methyl group Chemical group [H]C1=C([H])C([H])=C([H])C(=N1)C([H])([H])* 0.000 description 1
VHMICKWLTGFITH-UHFFFAOYSA-N 2H-isoindole Chemical compound C1=CC=CC2=CNC=C21 VHMICKWLTGFITH-UHFFFAOYSA-N 0.000 description 1
JZIBVTUXIVIFGC-UHFFFAOYSA-N 2H-pyrrole Chemical compound C1C=CC=N1 JZIBVTUXIVIFGC-UHFFFAOYSA-N 0.000 description 1
BMYNFMYTOJXKLE-UHFFFAOYSA-N 3-azaniumyl-2-hydroxypropanoate Chemical compound NCC(O)C(O)=O BMYNFMYTOJXKLE-UHFFFAOYSA-N 0.000 description 1
125000004975 3-butenyl group Chemical group C(CC=C)* 0.000 description 1
ZRPLANDPDWYOMZ-UHFFFAOYSA-N 3-cyclopentylpropionic acid Chemical compound OC(=O)CCC1CCCC1 ZRPLANDPDWYOMZ-UHFFFAOYSA-N 0.000 description 1
125000006201 3-phenylpropyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
UBOOKRVGOBKDMM-UHFFFAOYSA-N 3h-imidazo[4,5-c]pyridine Chemical compound C1=NC=C2NC=NC2=C1 UBOOKRVGOBKDMM-UHFFFAOYSA-N 0.000 description 1
UPKVIZJOHNISPP-UHFFFAOYSA-N 4-[(9-cyclohexyl-7,7-difluoro-5-methyl-6-oxo-8h-pyrimido[4,5-b][1,4]diazepin-2-yl)amino]-3-methoxy-n-(2-pyrrolidin-1-ylethyl)benzamide Chemical compound COC1=CC(C(=O)NCCN2CCCC2)=CC=C1NC(N=C12)=NC=C1N(C)C(=O)C(F)(F)CN2C1CCCCC1 UPKVIZJOHNISPP-UHFFFAOYSA-N 0.000 description 1
HPUYLEFODLVQBB-GOSISDBHSA-N 4-[(9-cyclohexyl-7,7-difluoro-5-methyl-6-oxo-8h-pyrimido[4,5-b][1,4]diazepin-2-yl)amino]-3-methoxy-n-[(3r)-1-methylpyrrolidin-3-yl]benzamide Chemical compound COC1=CC(C(=O)N[C@H]2CN(C)CC2)=CC=C1NC(N=C12)=NC=C1N(C)C(=O)C(F)(F)CN2C1CCCCC1 HPUYLEFODLVQBB-GOSISDBHSA-N 0.000 description 1
UDGKHARVIQZCRM-GOSISDBHSA-N 4-[(9-cyclohexyl-7,7-difluoro-5-methyl-6-oxo-8h-pyrimido[4,5-b][1,4]diazepin-2-yl)amino]-3-methoxy-n-[(3r)-piperidin-3-yl]benzamide Chemical compound COC1=CC(C(=O)N[C@H]2CNCCC2)=CC=C1NC(N=C12)=NC=C1N(C)C(=O)C(F)(F)CN2C1CCCCC1 UDGKHARVIQZCRM-GOSISDBHSA-N 0.000 description 1
JIWASSBNCQACGB-QGZVFWFLSA-N 4-[(9-cyclohexyl-7,7-difluoro-5-methyl-6-oxo-8h-pyrimido[4,5-b][1,4]diazepin-2-yl)amino]-3-methoxy-n-[(3r)-pyrrolidin-3-yl]benzamide Chemical compound COC1=CC(C(=O)N[C@H]2CNCC2)=CC=C1NC(N=C12)=NC=C1N(C)C(=O)C(F)(F)CN2C1CCCCC1 JIWASSBNCQACGB-QGZVFWFLSA-N 0.000 description 1
BZRCXGLJEKOMKS-IBGZPJMESA-N 4-[(9-cyclohexyl-7,7-difluoro-5-methyl-6-oxo-8h-pyrimido[4,5-b][1,4]diazepin-2-yl)amino]-3-methoxy-n-[(3s)-1-methylpiperidin-3-yl]benzamide Chemical compound COC1=CC(C(=O)N[C@@H]2CN(C)CCC2)=CC=C1NC(N=C12)=NC=C1N(C)C(=O)C(F)(F)CN2C1CCCCC1 BZRCXGLJEKOMKS-IBGZPJMESA-N 0.000 description 1
LNRJJXYBPKZKNF-UHFFFAOYSA-N 4-[(9-cyclohexyl-7,7-difluoro-5-methyl-6-oxo-8h-pyrimido[4,5-b][1,4]diazepin-2-yl)amino]-3-methoxy-n-[1-(2,2,2-trifluoroethyl)piperidin-4-yl]benzamide Chemical compound COC1=CC(C(=O)NC2CCN(CC(F)(F)F)CC2)=CC=C1NC(N=C12)=NC=C1N(C)C(=O)C(F)(F)CN2C1CCCCC1 LNRJJXYBPKZKNF-UHFFFAOYSA-N 0.000 description 1
DNJPAXPYOSESEY-UHFFFAOYSA-N 4-[(9-cyclohexyl-7,7-difluoro-5-methyl-6-oxo-8h-pyrimido[4,5-b][1,4]diazepin-2-yl)amino]-3-methoxy-n-methylbenzamide Chemical compound COC1=CC(C(=O)NC)=CC=C1NC1=NC=C(N(C)C(=O)C(F)(F)CN2C3CCCCC3)C2=N1 DNJPAXPYOSESEY-UHFFFAOYSA-N 0.000 description 1
QNFJIRYQUCZBSX-UHFFFAOYSA-N 4-[(9-cyclohexyl-7,7-difluoro-5-methyl-6-oxo-8h-pyrimido[4,5-b][1,4]diazepin-2-yl)amino]-3-methoxy-n-pyrrolidin-1-ylbenzamide Chemical compound COC1=CC(C(=O)NN2CCCC2)=CC=C1NC(N=C12)=NC=C1N(C)C(=O)C(F)(F)CN2C1CCCCC1 QNFJIRYQUCZBSX-UHFFFAOYSA-N 0.000 description 1
AGLAFVGBYPTFSF-UHFFFAOYSA-N 4-[(9-cyclohexyl-7,7-difluoro-5-methyl-6-oxo-8h-pyrimido[4,5-b][1,4]diazepin-2-yl)amino]-3-methoxybenzamide Chemical compound COC1=CC(C(N)=O)=CC=C1NC1=NC=C(N(C)C(=O)C(F)(F)CN2C3CCCCC3)C2=N1 AGLAFVGBYPTFSF-UHFFFAOYSA-N 0.000 description 1
FDEAOXUCYSKSBH-UHFFFAOYSA-N 4-[(9-cyclohexyl-7,7-difluoro-5-methyl-6-oxo-8h-pyrimido[4,5-b][1,4]diazepin-2-yl)amino]-n-[1-(2-hydroxyethyl)piperidin-4-yl]-3-methoxybenzamide Chemical compound COC1=CC(C(=O)NC2CCN(CCO)CC2)=CC=C1NC(N=C12)=NC=C1N(C)C(=O)C(F)(F)CN2C1CCCCC1 FDEAOXUCYSKSBH-UHFFFAOYSA-N 0.000 description 1
BIBMZPCNPDUSHJ-UHFFFAOYSA-N 4-[(9-cyclohexyl-7-ethyl-7-fluoro-5-methyl-6-oxo-8h-pyrimido[4,5-b][1,4]diazepin-2-yl)amino]-3-methoxy-n-(1-methylpiperidin-4-yl)benzamide Chemical compound C12=NC(NC=3C(=CC(=CC=3)C(=O)NC3CCN(C)CC3)OC)=NC=C2N(C)C(=O)C(CC)(F)CN1C1CCCCC1 BIBMZPCNPDUSHJ-UHFFFAOYSA-N 0.000 description 1
GWRSATNRNFYMDI-UHFFFAOYSA-N 4-[(9-cyclopentyl-7,7-difluoro-5-methyl-6-oxo-8h-pyrimido[4,5-b][1,4]diazepin-2-yl)amino]-2-fluoro-5-methoxy-n-(1-methylpiperidin-4-yl)benzamide Chemical compound FC=1C=C(NC=2N=C3N(C4CCCC4)CC(F)(F)C(=O)N(C)C3=CN=2)C(OC)=CC=1C(=O)NC1CCN(C)CC1 GWRSATNRNFYMDI-UHFFFAOYSA-N 0.000 description 1
VPBZFGFCOASXMG-UHFFFAOYSA-N 4-[(9-cyclopentyl-7,7-difluoro-5-methyl-6-oxo-8h-pyrimido[4,5-b][1,4]diazepin-2-yl)amino]-3-fluoro-5-methoxybenzoic acid Chemical compound COC1=CC(C(O)=O)=CC(F)=C1NC1=NC=C(N(C)C(=O)C(F)(F)CN2C3CCCC3)C2=N1 VPBZFGFCOASXMG-UHFFFAOYSA-N 0.000 description 1
BONXCAFEMZDKQU-UHFFFAOYSA-N 4-[(9-cyclopentyl-7,7-difluoro-5-methyl-6-oxo-8h-pyrimido[4,5-b][1,4]diazepin-2-yl)amino]-3-methoxy-n-(1-methylsulfonylpiperidin-4-yl)benzamide Chemical compound COC1=CC(C(=O)NC2CCN(CC2)S(C)(=O)=O)=CC=C1NC(N=C12)=NC=C1N(C)C(=O)C(F)(F)CN2C1CCCC1 BONXCAFEMZDKQU-UHFFFAOYSA-N 0.000 description 1
FHYRMGNMJYUJBJ-UHFFFAOYSA-N 4-[(9-cyclopentyl-7,7-difluoro-5-methyl-6-oxo-8h-pyrimido[4,5-b][1,4]diazepin-2-yl)amino]-3-methoxy-n-(2-pyrrolidin-1-ylethyl)benzamide Chemical compound COC1=CC(C(=O)NCCN2CCCC2)=CC=C1NC(N=C12)=NC=C1N(C)C(=O)C(F)(F)CN2C1CCCC1 FHYRMGNMJYUJBJ-UHFFFAOYSA-N 0.000 description 1
INRRBJHFKZXWEP-VCSGRIEYSA-N 4-[(9-cyclopentyl-7,7-difluoro-5-methyl-6-oxo-8h-pyrimido[4,5-b][1,4]diazepin-2-yl)amino]-3-methoxy-n-[(1s,5r)-8-methyl-8-azabicyclo[3.2.1]octan-3-yl]benzamide Chemical compound C([C@]1(CC[C@@](C2)(N1C)[H])[H])C2NC(=O)C(C=C1OC)=CC=C1NC(N=C12)=NC=C1N(C)C(=O)C(F)(F)CN2C1CCCC1 INRRBJHFKZXWEP-VCSGRIEYSA-N 0.000 description 1
HLCDTULFFZETLA-UHFFFAOYSA-N 4-[(9-cyclopentyl-7,7-difluoro-5-methyl-6-oxo-8h-pyrimido[4,5-b][1,4]diazepin-2-yl)amino]-3-methoxy-n-[1-(2,2,2-trifluoroethyl)piperidin-4-yl]benzamide Chemical compound COC1=CC(C(=O)NC2CCN(CC(F)(F)F)CC2)=CC=C1NC(N=C12)=NC=C1N(C)C(=O)C(F)(F)CN2C1CCCC1 HLCDTULFFZETLA-UHFFFAOYSA-N 0.000 description 1
BTQNGTAMCLWLOP-UHFFFAOYSA-N 4-[(9-cyclopentyl-7,7-difluoro-5-methyl-6-oxo-8h-pyrimido[4,5-b][1,4]diazepin-2-yl)amino]-3-methoxy-n-methylbenzamide Chemical compound COC1=CC(C(=O)NC)=CC=C1NC1=NC=C(N(C)C(=O)C(F)(F)CN2C3CCCC3)C2=N1 BTQNGTAMCLWLOP-UHFFFAOYSA-N 0.000 description 1
YDOOBHGKRCSAML-UHFFFAOYSA-N 4-[(9-cyclopentyl-7,7-difluoro-5-methyl-6-oxo-8h-pyrimido[4,5-b][1,4]diazepin-2-yl)amino]-3-methoxy-n-pyrrolidin-1-ylbenzamide Chemical compound COC1=CC(C(=O)NN2CCCC2)=CC=C1NC(N=C12)=NC=C1N(C)C(=O)C(F)(F)CN2C1CCCC1 YDOOBHGKRCSAML-UHFFFAOYSA-N 0.000 description 1
DQJHTCZROXSXEZ-UHFFFAOYSA-N 4-[(9-cyclopentyl-7,7-difluoro-5-methyl-6-oxo-8h-pyrimido[4,5-b][1,4]diazepin-2-yl)amino]-3-methoxybenzoic acid Chemical compound COC1=CC(C(O)=O)=CC=C1NC1=NC=C(N(C)C(=O)C(F)(F)CN2C3CCCC3)C2=N1 DQJHTCZROXSXEZ-UHFFFAOYSA-N 0.000 description 1
JMTVQKMGWVDRNW-UHFFFAOYSA-N 4-[(9-cyclopentyl-7,7-difluoro-5-methyl-6-oxo-8h-pyrimido[4,5-b][1,4]diazepin-2-yl)amino]-n-(2-hydroxyethyl)-3-methoxybenzamide Chemical compound COC1=CC(C(=O)NCCO)=CC=C1NC1=NC=C(N(C)C(=O)C(F)(F)CN2C3CCCC3)C2=N1 JMTVQKMGWVDRNW-UHFFFAOYSA-N 0.000 description 1
WHKHOIVBTZDHNY-UHFFFAOYSA-N 4-[(9-cyclopentyl-7,7-difluoro-5-methyl-6-oxo-8h-pyrimido[4,5-b][1,4]diazepin-2-yl)amino]-n-[1-(2-hydroxyethyl)piperidin-4-yl]-3-methoxybenzamide Chemical compound COC1=CC(C(=O)NC2CCN(CCO)CC2)=CC=C1NC(N=C12)=NC=C1N(C)C(=O)C(F)(F)CN2C1CCCC1 WHKHOIVBTZDHNY-UHFFFAOYSA-N 0.000 description 1
BKISFVPZQDWMAG-UHFFFAOYSA-N 4-[(9-cyclopentyl-7,7-difluoro-5-methyl-6-oxo-8h-pyrimido[4,5-b][1,4]diazepin-2-yl)amino]-n-[4-(dimethylamino)cyclohexyl]-3-methoxybenzamide Chemical compound COC1=CC(C(=O)NC2CCC(CC2)N(C)C)=CC=C1NC(N=C12)=NC=C1N(C)C(=O)C(F)(F)CN2C1CCCC1 BKISFVPZQDWMAG-UHFFFAOYSA-N 0.000 description 1
JONSYJDXBWCVOL-UHFFFAOYSA-N 4-[(9-cyclopentyl-7-ethenyl-7-fluoro-5-methyl-6-oxo-8h-pyrimido[4,5-b][1,4]diazepin-2-yl)amino]-3-methoxybenzoic acid Chemical compound COC1=CC(C(O)=O)=CC=C1NC1=NC=C(N(C)C(=O)C(F)(CN2C3CCCC3)C=C)C2=N1 JONSYJDXBWCVOL-UHFFFAOYSA-N 0.000 description 1
NMRBMIFSCDGALF-UHFFFAOYSA-N 4-[(9-cyclopentyl-7-fluoro-5,7-dimethyl-6-oxo-8h-pyrimido[4,5-b][1,4]diazepin-2-yl)amino]-3-methoxy-n-(1-methylpiperidin-4-yl)benzamide Chemical compound COC1=CC(C(=O)NC2CCN(C)CC2)=CC=C1NC(N=C12)=NC=C1N(C)C(=O)C(C)(F)CN2C1CCCC1 NMRBMIFSCDGALF-UHFFFAOYSA-N 0.000 description 1
HOYCBMBOVBGXOR-SSEXGKCCSA-N 4-[[(7r)-9-cyclohexyl-7-ethynyl-7-fluoro-5-methyl-6-oxo-8h-pyrimido[4,5-b][1,4]diazepin-2-yl]amino]-3-methoxy-n-(1-methylpiperidin-4-yl)benzamide Chemical compound C([C@@](F)(C(=O)N(C)C1=CN=C(N=C11)NC2=CC=C(C=C2OC)C(=O)NC2CCN(C)CC2)C#C)N1C1CCCCC1 HOYCBMBOVBGXOR-SSEXGKCCSA-N 0.000 description 1
FILLOSJEJCCSNM-HSZRJFAPSA-N 4-[[(7r)-9-cyclopentyl-7-ethenyl-7-fluoro-5-methyl-6-oxo-8h-pyrimido[4,5-b][1,4]diazepin-2-yl]amino]-2-fluoro-5-methoxybenzoic acid Chemical compound COC1=CC(C(O)=O)=C(F)C=C1NC1=NC=C(N(C)C(=O)[C@](F)(CN2C3CCCC3)C=C)C2=N1 FILLOSJEJCCSNM-HSZRJFAPSA-N 0.000 description 1
NQOOFRFMCZPURE-DNOBIOAJSA-N 4-[[(7r)-9-cyclopentyl-7-ethynyl-7-fluoro-5-methyl-6-oxo-8h-pyrimido[4,5-b][1,4]diazepin-2-yl]amino]-3-fluoro-n-[(3r)-piperidin-3-yl]benzamide Chemical compound O=C([C@@](F)(C#C)CN(C1=N2)C3CCCC3)N(C)C1=CN=C2NC(C(=C1)F)=CC=C1C(=O)N[C@@H]1CCCNC1 NQOOFRFMCZPURE-DNOBIOAJSA-N 0.000 description 1
HOYCBMBOVBGXOR-PMERELPUSA-N 4-[[(7s)-9-cyclohexyl-7-ethynyl-7-fluoro-5-methyl-6-oxo-8h-pyrimido[4,5-b][1,4]diazepin-2-yl]amino]-3-methoxy-n-(1-methylpiperidin-4-yl)benzamide Chemical compound C([C@](F)(C(=O)N(C)C1=CN=C(N=C11)NC2=CC=C(C=C2OC)C(=O)NC2CCN(C)CC2)C#C)N1C1CCCCC1 HOYCBMBOVBGXOR-PMERELPUSA-N 0.000 description 1
KRPORFVRNWPFMV-LJAQVGFWSA-N 4-[[(7s)-9-cyclopentyl-7-ethynyl-7-fluoro-5-methyl-6-oxo-8h-pyrimido[4,5-b][1,4]diazepin-2-yl]amino]-3-methoxy-n-(1-methylpiperidin-4-yl)benzamide Chemical compound C([C@](F)(C(=O)N(C)C1=CN=C(N=C11)NC2=CC=C(C=C2OC)C(=O)NC2CCN(C)CC2)C#C)N1C1CCCC1 KRPORFVRNWPFMV-LJAQVGFWSA-N 0.000 description 1
RJWBTWIBUIGANW-UHFFFAOYSA-N 4-chlorobenzenesulfonic acid Chemical compound OS(=O)(=O)C1=CC=C(Cl)C=C1 RJWBTWIBUIGANW-UHFFFAOYSA-N 0.000 description 1
JJTNLWSCFYERCK-UHFFFAOYSA-N 7h-pyrrolo[2,3-d]pyrimidine Chemical compound N1=CN=C2NC=CC2=C1 JJTNLWSCFYERCK-UHFFFAOYSA-N 0.000 description 1
GRLNQRDPTGISSD-UHFFFAOYSA-N 9-cyclopentyl-7,7-difluoro-2-(1h-indol-5-ylamino)-5-methyl-8h-pyrimido[4,5-b][1,4]diazepin-6-one Chemical compound C1C(F)(F)C(=O)N(C)C2=CN=C(NC=3C=C4C=CNC4=CC=3)N=C2N1C1CCCC1 GRLNQRDPTGISSD-UHFFFAOYSA-N 0.000 description 1
KNIWRDSSSDRONC-UHFFFAOYSA-N 9-cyclopentyl-7,7-difluoro-5-methyl-2-[[3-(1,2,3,6-tetrahydropyridin-4-yl)-1h-indol-5-yl]amino]-8h-pyrimido[4,5-b][1,4]diazepin-6-one Chemical compound N1=C2N(C3CCCC3)CC(F)(F)C(=O)N(C)C2=CN=C1NC(C=C12)=CC=C1NC=C2C1=CCNCC1 KNIWRDSSSDRONC-UHFFFAOYSA-N 0.000 description 1
FSHURBQASBLAPO-WDSKDSINSA-N Ala-Met Chemical compound CSCC[C@@H](C(O)=O)NC(=O)[C@H](C)N FSHURBQASBLAPO-WDSKDSINSA-N 0.000 description 1
OMNVYXHOSHNURL-WPRPVWTQSA-N Ala-Phe Chemical group C[C@H](N)C(=O)N[C@H](C(O)=O)CC1=CC=CC=C1 OMNVYXHOSHNURL-WPRPVWTQSA-N 0.000 description 1
239000004475 Arginine Substances 0.000 description 1
201000001320 Atherosclerosis Diseases 0.000 description 1
102100032306 Aurora kinase B Human genes 0.000 description 1
OUFRHRLDTHNWGD-UHFFFAOYSA-N C12=CC=C(N1)C=C1C=CC(=N1)C=C1C=CC(N1)=CC=1C=CC(N1)=C2.N2=CN=CC1=CC=CC=C21 Chemical compound C12=CC=C(N1)C=C1C=CC(=N1)C=C1C=CC(N1)=CC=1C=CC(N1)=C2.N2=CN=CC1=CC=CC=C21 OUFRHRLDTHNWGD-UHFFFAOYSA-N 0.000 description 1
YEGHHUBBDYZWDD-UHFFFAOYSA-N COC1=CC(C(=O)NC2CCN(C)CC2)=CC=C1NC(N=1)=NC=C(N2C=NN=C2C(F)(F)C2)C=1N2C1CCCC1 Chemical compound COC1=CC(C(=O)NC2CCN(C)CC2)=CC=C1NC(N=1)=NC=C(N2C=NN=C2C(F)(F)C2)C=1N2C1CCCC1 YEGHHUBBDYZWDD-UHFFFAOYSA-N 0.000 description 1
MPUTXDITICWTEY-UHFFFAOYSA-N COC1=CC(C(=O)NC2CCN(C)CC2)=CC=C1NC(N=1)=NC=C(N2N=CN=C2C(F)(F)C2)C=1N2C1CCCC1 Chemical compound COC1=CC(C(=O)NC2CCN(C)CC2)=CC=C1NC(N=1)=NC=C(N2N=CN=C2C(F)(F)C2)C=1N2C1CCCC1 MPUTXDITICWTEY-UHFFFAOYSA-N 0.000 description 1
QHIFGCQEDCOCNK-UHFFFAOYSA-N COC1=CC(C(=O)NC2CCN(C)CC2)=CC=C1NC(N=1)=NC=C(N2N=NN=C2C(F)(F)C2)C=1N2C1CCCC1 Chemical compound COC1=CC(C(=O)NC2CCN(C)CC2)=CC=C1NC(N=1)=NC=C(N2N=NN=C2C(F)(F)C2)C=1N2C1CCCC1 QHIFGCQEDCOCNK-UHFFFAOYSA-N 0.000 description 1
101100381481 Caenorhabditis elegans baz-2 gene Proteins 0.000 description 1
ZEOWTGPWHLSLOG-UHFFFAOYSA-N Cc1ccc(cc1-c1ccc2c(n[nH]c2c1)-c1cnn(c1)C1CC1)C(=O)Nc1cccc(c1)C(F)(F)F Chemical compound Cc1ccc(cc1-c1ccc2c(n[nH]c2c1)-c1cnn(c1)C1CC1)C(=O)Nc1cccc(c1)C(F)(F)F ZEOWTGPWHLSLOG-UHFFFAOYSA-N 0.000 description 1
229910052684 Cerium Inorganic materials 0.000 description 1
WBYWAXJHAXSJNI-SREVYHEPSA-N Cinnamic acid Chemical compound OC(=O)\C=C/C1=CC=CC=C1 WBYWAXJHAXSJNI-SREVYHEPSA-N 0.000 description 1
206010009944 Colon cancer Diseases 0.000 description 1
229940126062 Compound A Drugs 0.000 description 1
108010024986 Cyclin-Dependent Kinase 2 Proteins 0.000 description 1
108010025464 Cyclin-Dependent Kinase 4 Proteins 0.000 description 1
108010025468 Cyclin-Dependent Kinase 6 Proteins 0.000 description 1
102100032857 Cyclin-dependent kinase 1 Human genes 0.000 description 1
101710106279 Cyclin-dependent kinase 1 Proteins 0.000 description 1
102100036239 Cyclin-dependent kinase 2 Human genes 0.000 description 1
102100036252 Cyclin-dependent kinase 4 Human genes 0.000 description 1
102100026804 Cyclin-dependent kinase 6 Human genes 0.000 description 1
102000010831 Cytoskeletal Proteins Human genes 0.000 description 1
108010037414 Cytoskeletal Proteins Proteins 0.000 description 1
QNAYBMKLOCPYGJ-UHFFFAOYSA-N D-alpha-Ala Natural products CC([NH3+])C([O-])=O QNAYBMKLOCPYGJ-UHFFFAOYSA-N 0.000 description 1
RGHNJXZEOKUKBD-UHFFFAOYSA-N D-gluconic acid Natural products OCC(O)C(O)C(O)C(O)C(O)=O RGHNJXZEOKUKBD-UHFFFAOYSA-N 0.000 description 1
101100503636 Danio rerio fyna gene Proteins 0.000 description 1
101100481404 Danio rerio tie1 gene Proteins 0.000 description 1
101100481408 Danio rerio tie2 gene Proteins 0.000 description 1
101100314281 Danio rerio trappc11 gene Proteins 0.000 description 1
101100261976 Drosophila melanogaster trk gene Proteins 0.000 description 1
102100030011 Endoribonuclease Human genes 0.000 description 1
101710199605 Endoribonuclease Proteins 0.000 description 1
241001125671 Eretmochelys imbricata Species 0.000 description 1
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
239000005977 Ethylene Substances 0.000 description 1
108010007457 Extracellular Signal-Regulated MAP Kinases Proteins 0.000 description 1
101150036586 FES gene Proteins 0.000 description 1
101150017750 FGFRL1 gene Proteins 0.000 description 1
101150018370 FRK gene Proteins 0.000 description 1
101150018272 FYN gene Proteins 0.000 description 1
101150040897 Fgr gene Proteins 0.000 description 1
102100023593 Fibroblast growth factor receptor 1 Human genes 0.000 description 1
101710182386 Fibroblast growth factor receptor 1 Proteins 0.000 description 1
102100023600 Fibroblast growth factor receptor 2 Human genes 0.000 description 1
101710182389 Fibroblast growth factor receptor 2 Proteins 0.000 description 1
102100027842 Fibroblast growth factor receptor 3 Human genes 0.000 description 1
101710182396 Fibroblast growth factor receptor 3 Proteins 0.000 description 1
102100027844 Fibroblast growth factor receptor 4 Human genes 0.000 description 1
102100026149 Fibroblast growth factor receptor-like 1 Human genes 0.000 description 1
241000287828 Gallus gallus Species 0.000 description 1
JBCLFWXMTIKCCB-VIFPVBQESA-N Gly-Phe Chemical group NCC(=O)N[C@H](C(O)=O)CC1=CC=CC=C1 JBCLFWXMTIKCCB-VIFPVBQESA-N 0.000 description 1
239000004471 Glycine Substances 0.000 description 1
102000009465 Growth Factor Receptors Human genes 0.000 description 1
108010009202 Growth Factor Receptors Proteins 0.000 description 1
JBCLFWXMTIKCCB-UHFFFAOYSA-N H-Gly-Phe-OH Natural products NCC(=O)NC(C(O)=O)CC1=CC=CC=C1 JBCLFWXMTIKCCB-UHFFFAOYSA-N 0.000 description 1
101150004849 HCK gene Proteins 0.000 description 1
208000005176 Hepatitis C Diseases 0.000 description 1
NLDMNSXOCDLTTB-UHFFFAOYSA-N Heterophylliin A Natural products O1C2COC(=O)C3=CC(O)=C(O)C(O)=C3C3=C(O)C(O)=C(O)C=C3C(=O)OC2C(OC(=O)C=2C=C(O)C(O)=C(O)C=2)C(O)C1OC(=O)C1=CC(O)=C(O)C(O)=C1 NLDMNSXOCDLTTB-UHFFFAOYSA-N 0.000 description 1
101000798306 Homo sapiens Aurora kinase B Proteins 0.000 description 1
101000917134 Homo sapiens Fibroblast growth factor receptor 4 Proteins 0.000 description 1
101000916644 Homo sapiens Macrophage colony-stimulating factor 1 receptor Proteins 0.000 description 1
101000692455 Homo sapiens Platelet-derived growth factor receptor beta Proteins 0.000 description 1
101000878540 Homo sapiens Protein-tyrosine kinase 2-beta Proteins 0.000 description 1
101000729945 Homo sapiens Serine/threonine-protein kinase PLK2 Proteins 0.000 description 1
101000691614 Homo sapiens Serine/threonine-protein kinase PLK3 Proteins 0.000 description 1
101000582914 Homo sapiens Serine/threonine-protein kinase PLK4 Proteins 0.000 description 1
101000922131 Homo sapiens Tyrosine-protein kinase CSK Proteins 0.000 description 1
PMMYEEVYMWASQN-DMTCNVIQSA-N Hydroxyproline Chemical compound O[C@H]1CN[C@H](C(O)=O)C1 PMMYEEVYMWASQN-DMTCNVIQSA-N 0.000 description 1
206010020751 Hypersensitivity Diseases 0.000 description 1
206010061218 Inflammation Diseases 0.000 description 1
102000004310 Ion Channels Human genes 0.000 description 1
108090000862 Ion Channels Proteins 0.000 description 1
AHLPHDHHMVZTML-BYPYZUCNSA-N L-Ornithine Chemical compound NCCC[C@H](N)C(O)=O AHLPHDHHMVZTML-BYPYZUCNSA-N 0.000 description 1
QNAYBMKLOCPYGJ-REOHCLBHSA-N L-alanine Chemical compound C[C@H](N)C(O)=O QNAYBMKLOCPYGJ-REOHCLBHSA-N 0.000 description 1
125000000998 L-alanino group Chemical group [H]N([*])[C@](C([H])([H])[H])([H])C(=O)O[H] 0.000 description 1
DEFJQIDDEAULHB-IMJSIDKUSA-N L-alanyl-L-alanine Chemical compound C[C@H](N)C(=O)N[C@@H](C)C(O)=O DEFJQIDDEAULHB-IMJSIDKUSA-N 0.000 description 1
UKAUYVFTDYCKQA-VKHMYHEASA-N L-homoserine Chemical compound OC(=O)[C@@H](N)CCO UKAUYVFTDYCKQA-VKHMYHEASA-N 0.000 description 1
125000000393 L-methionino group Chemical group [H]OC(=O)[C@@]([H])(N([H])[*])C([H])([H])C(SC([H])([H])[H])([H])[H] 0.000 description 1
QIVBCDIJIAJPQS-VIFPVBQESA-N L-tryptophane Chemical compound C1=CC=C2C(C[C@H](N)C(O)=O)=CNC2=C1 QIVBCDIJIAJPQS-VIFPVBQESA-N 0.000 description 1
125000000510 L-tryptophano group Chemical group [H]C1=C([H])C([H])=C2N([H])C([H])=C(C([H])([H])[C@@]([H])(C(O[H])=O)N([H])[*])C2=C1[H] 0.000 description 1
NTISAKGPIGTIJJ-IUCAKERBSA-N Leu-Met Chemical compound CSCC[C@@H](C(O)=O)NC(=O)[C@@H](N)CC(C)C NTISAKGPIGTIJJ-IUCAKERBSA-N 0.000 description 1
ROHFNLRQFUQHCH-UHFFFAOYSA-N Leucine Natural products CC(C)CC(N)C(O)=O ROHFNLRQFUQHCH-UHFFFAOYSA-N 0.000 description 1
102100028198 Macrophage colony-stimulating factor 1 receptor Human genes 0.000 description 1
ZYTPOUNUXRBYGW-YUMQZZPRSA-N Met-Met Chemical compound CSCC[C@H]([NH3+])C(=O)N[C@H](C([O-])=O)CCSC ZYTPOUNUXRBYGW-YUMQZZPRSA-N 0.000 description 1
TXXHDPDFNKHHGW-CCAGOZQPSA-N Muconic acid Natural products OC(=O)\C=C/C=C\C(O)=O TXXHDPDFNKHHGW-CCAGOZQPSA-N 0.000 description 1
101100091501 Mus musculus Ros1 gene Proteins 0.000 description 1
101100481410 Mus musculus Tek gene Proteins 0.000 description 1
101100481406 Mus musculus Tie1 gene Proteins 0.000 description 1
101100268066 Mus musculus Zap70 gene Proteins 0.000 description 1
MBBZMMPHUWSWHV-BDVNFPICSA-N N-methylglucamine Chemical compound CNC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO MBBZMMPHUWSWHV-BDVNFPICSA-N 0.000 description 1
238000005481 NMR spectroscopy Methods 0.000 description 1
GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 1
JCXJVPUVTGWSNB-UHFFFAOYSA-N Nitrogen dioxide Chemical compound O=[N]=O JCXJVPUVTGWSNB-UHFFFAOYSA-N 0.000 description 1
102000043276 Oncogene Human genes 0.000 description 1
AHLPHDHHMVZTML-UHFFFAOYSA-N Orn-delta-NH2 Natural products NCCCC(N)C(O)=O AHLPHDHHMVZTML-UHFFFAOYSA-N 0.000 description 1
UTJLXEIPEHZYQJ-UHFFFAOYSA-N Ornithine Natural products OC(=O)C(C)CCCN UTJLXEIPEHZYQJ-UHFFFAOYSA-N 0.000 description 1
101100381429 Oryza sativa subsp. japonica BADH2 gene Proteins 0.000 description 1
102000038030 PI3Ks Human genes 0.000 description 1
108091007960 PI3Ks Proteins 0.000 description 1
101150054473 PTK2 gene Proteins 0.000 description 1
OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
102100026547 Platelet-derived growth factor receptor beta Human genes 0.000 description 1
229940122166 Polo-like kinase inhibitor Drugs 0.000 description 1
108090000315 Protein Kinase C Proteins 0.000 description 1
102100037787 Protein-tyrosine kinase 2-beta Human genes 0.000 description 1
102000016971 Proto-Oncogene Proteins c-kit Human genes 0.000 description 1
108010014608 Proto-Oncogene Proteins c-kit Proteins 0.000 description 1
101150040459 RAS gene Proteins 0.000 description 1
101100372762 Rattus norvegicus Flt1 gene Proteins 0.000 description 1
101100517381 Rattus norvegicus Ntrk1 gene Proteins 0.000 description 1
108020004511 Recombinant DNA Proteins 0.000 description 1
101100091511 Rhizobium radiobacter ros gene Proteins 0.000 description 1
101150001535 SRC gene Proteins 0.000 description 1
101100537955 Schizosaccharomyces pombe (strain 972 / ATCC 24843) trk1 gene Proteins 0.000 description 1
MTCFGRXMJLQNBG-UHFFFAOYSA-N Serine Natural products OCC(N)C(O)=O MTCFGRXMJLQNBG-UHFFFAOYSA-N 0.000 description 1
101710113029 Serine/threonine-protein kinase Proteins 0.000 description 1
102100031462 Serine/threonine-protein kinase PLK2 Human genes 0.000 description 1
102100026209 Serine/threonine-protein kinase PLK3 Human genes 0.000 description 1
102100030267 Serine/threonine-protein kinase PLK4 Human genes 0.000 description 1
235000021355 Stearic acid Nutrition 0.000 description 1
KDYFGRWQOYBRFD-UHFFFAOYSA-N Succinic acid Natural products OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 1
229940100389 Sulfonylurea Drugs 0.000 description 1
101001045447 Synechocystis sp. (strain PCC 6803 / Kazusa) Sensor histidine kinase Hik2 Proteins 0.000 description 1
FEWJPZIEWOKRBE-UHFFFAOYSA-N Tartaric acid Natural products [H+].[H+].[O-]C(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-N 0.000 description 1
FZWLAAWBMGSTSO-UHFFFAOYSA-N Thiazole Chemical compound C1=CSC=N1 FZWLAAWBMGSTSO-UHFFFAOYSA-N 0.000 description 1
108091023040 Transcription factor Proteins 0.000 description 1
102000040945 Transcription factor Human genes 0.000 description 1
GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 1
QIVBCDIJIAJPQS-UHFFFAOYSA-N Tryptophan Natural products C1=CC=C2C(CC(N)C(O)=O)=CNC2=C1 QIVBCDIJIAJPQS-UHFFFAOYSA-N 0.000 description 1
102100031167 Tyrosine-protein kinase CSK Human genes 0.000 description 1
108010053100 Vascular Endothelial Growth Factor Receptor-3 Proteins 0.000 description 1
102000016663 Vascular Endothelial Growth Factor Receptor-3 Human genes 0.000 description 1
JLYXEQPCPLGLGP-UHFFFAOYSA-N [4-[(9-cyclopentyl-7,7-difluoro-5-methyl-6,8-dihydropyrimido[4,5-b][1,4]diazepin-2-yl)amino]-3-methoxyphenyl]methanol Chemical compound COC1=CC(CO)=CC=C1NC1=NC=C(N(C)CC(F)(F)CN2C3CCCC3)C2=N1 JLYXEQPCPLGLGP-UHFFFAOYSA-N 0.000 description 1
230000005856 abnormality Effects 0.000 description 1
150000001242 acetic acid derivatives Chemical class 0.000 description 1
230000002378 acidificating effect Effects 0.000 description 1
150000007513 acids Chemical class 0.000 description 1
239000004480 active ingredient Substances 0.000 description 1
235000004279 alanine Nutrition 0.000 description 1
108010056243 alanylalanine Proteins 0.000 description 1
108010011559 alanylphenylalanine Proteins 0.000 description 1
125000004450 alkenylene group Chemical group 0.000 description 1
230000029936 alkylation Effects 0.000 description 1
238000005804 alkylation reaction Methods 0.000 description 1
BJEPYKJPYRNKOW-UHFFFAOYSA-N alpha-hydroxysuccinic acid Natural products OC(=O)C(O)CC(O)=O BJEPYKJPYRNKOW-UHFFFAOYSA-N 0.000 description 1
WNROFYMDJYEPJX-UHFFFAOYSA-K aluminium hydroxide Chemical compound [OH-].[OH-].[OH-].[Al+3] WNROFYMDJYEPJX-UHFFFAOYSA-K 0.000 description 1
125000004103 aminoalkyl group Chemical group 0.000 description 1
230000033115 angiogenesis Effects 0.000 description 1
229940045988 antineoplastic drug protein kinase inhibitors Drugs 0.000 description 1
ODKSFYDXXFIFQN-UHFFFAOYSA-N arginine Natural products OC(=O)C(N)CCCNC(N)=N ODKSFYDXXFIFQN-UHFFFAOYSA-N 0.000 description 1
125000003710 aryl alkyl group Chemical group 0.000 description 1
125000004391 aryl sulfonyl group Chemical group 0.000 description 1
229940009098 aspartate Drugs 0.000 description 1
235000003704 aspartic acid Nutrition 0.000 description 1
208000006673 asthma Diseases 0.000 description 1
125000000852 azido group Chemical group *N=[N+]=[N-] 0.000 description 1
RFRXIWQYSOIBDI-UHFFFAOYSA-N benzarone Chemical compound CCC=1OC2=CC=CC=C2C=1C(=O)C1=CC=C(O)C=C1 RFRXIWQYSOIBDI-UHFFFAOYSA-N 0.000 description 1
125000000051 benzyloxy group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])O* 0.000 description 1
UCMIRNVEIXFBKS-UHFFFAOYSA-N beta-alanine Chemical compound NCCC(O)=O UCMIRNVEIXFBKS-UHFFFAOYSA-N 0.000 description 1
OQFSQFPPLPISGP-UHFFFAOYSA-N beta-carboxyaspartic acid Natural products OC(=O)C(N)C(C(O)=O)C(O)=O OQFSQFPPLPISGP-UHFFFAOYSA-N 0.000 description 1
ZESXVLLAIXOYKB-UHFFFAOYSA-N bicyclo[2.2.1]heptan-7-one Chemical compound C1CC2CCC1C2=O ZESXVLLAIXOYKB-UHFFFAOYSA-N 0.000 description 1
GPRLTFBKWDERLU-UHFFFAOYSA-N bicyclo[2.2.2]octane Chemical compound C1CC2CCC1CC2 GPRLTFBKWDERLU-UHFFFAOYSA-N 0.000 description 1
230000008827 biological function Effects 0.000 description 1
230000033228 biological regulation Effects 0.000 description 1
230000015572 biosynthetic process Effects 0.000 description 1
210000004369 blood Anatomy 0.000 description 1
210000000601 blood cell Anatomy 0.000 description 1
210000000481 breast Anatomy 0.000 description 1
229910052794 bromium Inorganic materials 0.000 description 1
125000001246 bromo group Chemical group Br* 0.000 description 1
KDYFGRWQOYBRFD-NUQCWPJISA-N butanedioic acid Chemical compound O[14C](=O)CC[14C](O)=O KDYFGRWQOYBRFD-NUQCWPJISA-N 0.000 description 1
125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
AXCZMVOFGPJBDE-UHFFFAOYSA-L calcium dihydroxide Chemical compound [OH-].[OH-].[Ca+2] AXCZMVOFGPJBDE-UHFFFAOYSA-L 0.000 description 1
239000000920 calcium hydroxide Substances 0.000 description 1
229910001861 calcium hydroxide Inorganic materials 0.000 description 1
125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 description 1
125000004452 carbocyclyl group Chemical group 0.000 description 1
CREMABGTGYGIQB-UHFFFAOYSA-N carbon carbon Chemical group C.C CREMABGTGYGIQB-UHFFFAOYSA-N 0.000 description 1
229910002091 carbon monoxide Inorganic materials 0.000 description 1
238000006555 catalytic reaction Methods 0.000 description 1
230000030833 cell death Effects 0.000 description 1
230000032823 cell division Effects 0.000 description 1
230000004663 cell proliferation Effects 0.000 description 1
230000001413 cellular effect Effects 0.000 description 1
230000033077 cellular process Effects 0.000 description 1
ZMIGMASIKSOYAM-UHFFFAOYSA-N cerium Chemical compound [Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce] ZMIGMASIKSOYAM-UHFFFAOYSA-N 0.000 description 1
SFZULDYEOVSIKM-UHFFFAOYSA-N chembl321317 Chemical compound C1=CC(C(=N)NO)=CC=C1C1=CC=C(C=2C=CC(=CC=2)C(=N)NO)O1 SFZULDYEOVSIKM-UHFFFAOYSA-N 0.000 description 1
239000000460 chlorine Substances 0.000 description 1
229910052801 chlorine Inorganic materials 0.000 description 1
210000000349 chromosome Anatomy 0.000 description 1
235000013985 cinnamic acid Nutrition 0.000 description 1
229930016911 cinnamic acid Natural products 0.000 description 1
229960004106 citric acid Drugs 0.000 description 1
235000015165 citric acid Nutrition 0.000 description 1
150000001860 citric acid derivatives Chemical class 0.000 description 1
210000001072 colon Anatomy 0.000 description 1
208000029742 colonic neoplasm Diseases 0.000 description 1
125000001995 cyclobutyl group Chemical group [H]C1([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 1
ZXIJMRYMVAMXQP-UHFFFAOYSA-N cycloheptene Chemical compound C1CCC=CCC1 ZXIJMRYMVAMXQP-UHFFFAOYSA-N 0.000 description 1
125000000596 cyclohexenyl group Chemical group C1(=CCCCC1)* 0.000 description 1
GCFAUZGWPDYAJN-UHFFFAOYSA-N cyclohexyl 3-phenylprop-2-enoate Chemical compound C=1C=CC=CC=1C=CC(=O)OC1CCCCC1 GCFAUZGWPDYAJN-UHFFFAOYSA-N 0.000 description 1
125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
HCAJEUSONLESMK-UHFFFAOYSA-N cyclohexylsulfamic acid Chemical compound OS(=O)(=O)NC1CCCCC1 HCAJEUSONLESMK-UHFFFAOYSA-N 0.000 description 1
WJTCGQSWYFHTAC-UHFFFAOYSA-N cyclooctane Chemical compound C1CCCCCCC1 WJTCGQSWYFHTAC-UHFFFAOYSA-N 0.000 description 1
239000004914 cyclooctane Substances 0.000 description 1
URYYVOIYTNXXBN-UPHRSURJSA-N cyclooctene Chemical compound C1CCC\C=C/CC1 URYYVOIYTNXXBN-UPHRSURJSA-N 0.000 description 1
239000004913 cyclooctene Substances 0.000 description 1
XUJNEKJLAYXESH-UHFFFAOYSA-N cysteine Natural products SCC(N)C(O)=O XUJNEKJLAYXESH-UHFFFAOYSA-N 0.000 description 1
235000018417 cysteine Nutrition 0.000 description 1
239000000824 cytostatic agent Substances 0.000 description 1
230000001085 cytostatic effect Effects 0.000 description 1
125000006612 decyloxy group Chemical group 0.000 description 1
125000005070 decynyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C#C* 0.000 description 1
230000002950 deficient Effects 0.000 description 1
125000004663 dialkyl amino group Chemical group 0.000 description 1
ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 description 1
150000004862 dioxolanes Chemical class 0.000 description 1
BEQVQKJCLJBTKZ-UHFFFAOYSA-N diphenylphosphinic acid Chemical group C=1C=CC=CC=1P(=O)(O)C1=CC=CC=C1 BEQVQKJCLJBTKZ-UHFFFAOYSA-N 0.000 description 1
230000006806 disease prevention Effects 0.000 description 1
238000010494 dissociation reaction Methods 0.000 description 1
230000005593 dissociations Effects 0.000 description 1
PMMYEEVYMWASQN-UHFFFAOYSA-N dl-hydroxyproline Natural products OC1C[NH2+]C(C([O-])=O)C1 PMMYEEVYMWASQN-UHFFFAOYSA-N 0.000 description 1
MOTZDAYCYVMXPC-UHFFFAOYSA-N dodecyl hydrogen sulfate Chemical compound CCCCCCCCCCCCOS(O)(=O)=O MOTZDAYCYVMXPC-UHFFFAOYSA-N 0.000 description 1
229940043264 dodecyl sulfate Drugs 0.000 description 1
239000002552 dosage form Substances 0.000 description 1
230000008482 dysregulation Effects 0.000 description 1
230000008030 elimination Effects 0.000 description 1
238000003379 elimination reaction Methods 0.000 description 1
230000007613 environmental effect Effects 0.000 description 1
102000052116 epidermal growth factor receptor activity proteins Human genes 0.000 description 1
108700015053 epidermal growth factor receptor activity proteins Proteins 0.000 description 1
AFAXGSQYZLGZPG-UHFFFAOYSA-N ethanedisulfonic acid Chemical compound OS(=O)(=O)CCS(O)(=O)=O AFAXGSQYZLGZPG-UHFFFAOYSA-N 0.000 description 1
125000003754 ethoxycarbonyl group Chemical group C(=O)(OCC)* 0.000 description 1
125000000816 ethylene group Chemical group [H]C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
RMBPEFMHABBEKP-UHFFFAOYSA-N fluorene Chemical compound C1=CC=C2C3=C[CH]C=CC3=CC2=C1 RMBPEFMHABBEKP-UHFFFAOYSA-N 0.000 description 1
239000011737 fluorine Substances 0.000 description 1
239000001530 fumaric acid Substances 0.000 description 1
235000011087 fumaric acid Nutrition 0.000 description 1
102000034356 gene-regulatory proteins Human genes 0.000 description 1
108091006104 gene-regulatory proteins Proteins 0.000 description 1
229940114119 gentisate Drugs 0.000 description 1
239000000174 gluconic acid Substances 0.000 description 1
235000012208 gluconic acid Nutrition 0.000 description 1
108010067216 glycyl-glycyl-glycine Proteins 0.000 description 1
YMAWOPBAYDPSLA-UHFFFAOYSA-N glycylglycine Chemical group [NH3+]CC(=O)NCC([O-])=O YMAWOPBAYDPSLA-UHFFFAOYSA-N 0.000 description 1
108010081551 glycylphenylalanine Proteins 0.000 description 1
210000004565 granule cell Anatomy 0.000 description 1
150000002390 heteroarenes Chemical class 0.000 description 1
125000004446 heteroarylalkyl group Chemical group 0.000 description 1
125000006038 hexenyl group Chemical group 0.000 description 1
238000004128 high performance liquid chromatography Methods 0.000 description 1
229940088597 hormone Drugs 0.000 description 1
239000005556 hormone Substances 0.000 description 1
150000004677 hydrates Chemical class 0.000 description 1
238000007327 hydrogenolysis reaction Methods 0.000 description 1
229960002591 hydroxyproline Drugs 0.000 description 1
UTCSSFWDNNEEBH-UHFFFAOYSA-N imidazo[1,2-a]pyridine Chemical compound C1=CC=CC2=NC=CN21 UTCSSFWDNNEEBH-UHFFFAOYSA-N 0.000 description 1
INSWZAQOISIYDT-UHFFFAOYSA-N imidazo[1,2-a]pyrimidine Chemical compound C1=CC=NC2=NC=CN21 INSWZAQOISIYDT-UHFFFAOYSA-N 0.000 description 1
PQWQQQGKMHENOC-UHFFFAOYSA-N imidazo[1,2-c]pyrimidine Chemical compound C1=NC=CC2=NC=CN21 PQWQQQGKMHENOC-UHFFFAOYSA-N 0.000 description 1
JMANUKZDKDKBJP-UHFFFAOYSA-N imidazo[1,5-a]pyridine Chemical compound C1=CC=CC2=CN=CN21 JMANUKZDKDKBJP-UHFFFAOYSA-N 0.000 description 1
LXYHLTOJFGNEKG-UHFFFAOYSA-N imidazo[1,5-a]pyrimidine Chemical compound C1=CC=NC2=CN=CN21 LXYHLTOJFGNEKG-UHFFFAOYSA-N 0.000 description 1
AGYYYBIAZFILKT-UHFFFAOYSA-N imidazo[1,5-c]pyrimidine Chemical compound C1=NC=CC2=CN=CN21 AGYYYBIAZFILKT-UHFFFAOYSA-N 0.000 description 1
210000000987 immune system Anatomy 0.000 description 1
JYGFTBXVXVMTGB-UHFFFAOYSA-N indolin-2-one Chemical compound C1=CC=C2NC(=O)CC2=C1 JYGFTBXVXVMTGB-UHFFFAOYSA-N 0.000 description 1
230000004054 inflammatory process Effects 0.000 description 1
239000004615 ingredient Substances 0.000 description 1
238000007913 intrathecal administration Methods 0.000 description 1
229910052740 iodine Inorganic materials 0.000 description 1
125000002346 iodo group Chemical group I* 0.000 description 1
125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
125000000654 isopropylidene group Chemical group C(C)(C)=* 0.000 description 1
125000005956 isoquinolyl group Chemical group 0.000 description 1
ZLTPDFXIESTBQG-UHFFFAOYSA-N isothiazole Chemical compound C=1C=NSC=1 ZLTPDFXIESTBQG-UHFFFAOYSA-N 0.000 description 1
230000000155 isotopic effect Effects 0.000 description 1
150000002561 ketenes Chemical class 0.000 description 1
150000003893 lactate salts Chemical class 0.000 description 1
239000004310 lactic acid Substances 0.000 description 1
235000014655 lactic acid Nutrition 0.000 description 1
229910052746 lanthanum Inorganic materials 0.000 description 1
FZLIPJUXYLNCLC-UHFFFAOYSA-N lanthanum atom Chemical compound [La] FZLIPJUXYLNCLC-UHFFFAOYSA-N 0.000 description 1
108010091871 leucylmethionine Proteins 0.000 description 1
230000000670 limiting effect Effects 0.000 description 1
239000002502 liposome Substances 0.000 description 1
239000011976 maleic acid Substances 0.000 description 1
239000001630 malic acid Substances 0.000 description 1
235000011090 malic acid Nutrition 0.000 description 1
IWYDHOAUDWTVEP-UHFFFAOYSA-N mandelic acid Chemical compound OC(=O)C(O)C1=CC=CC=C1 IWYDHOAUDWTVEP-UHFFFAOYSA-N 0.000 description 1
229960002510 mandelic acid Drugs 0.000 description 1
238000004949 mass spectrometry Methods 0.000 description 1
239000000463 material Substances 0.000 description 1
230000002503 metabolic effect Effects 0.000 description 1
230000004060 metabolic process Effects 0.000 description 1
229940098779 methanesulfonic acid Drugs 0.000 description 1
108010085203 methionylmethionine Proteins 0.000 description 1
UZKWTJUDCOPSNM-UHFFFAOYSA-N methoxybenzene Substances CCCCOC=C UZKWTJUDCOPSNM-UHFFFAOYSA-N 0.000 description 1
WBYWAXJHAXSJNI-UHFFFAOYSA-N methyl p-hydroxycinnamate Natural products OC(=O)C=CC1=CC=CC=C1 WBYWAXJHAXSJNI-UHFFFAOYSA-N 0.000 description 1
150000007522 mineralic acids Chemical class 0.000 description 1
230000000116 mitigating effect Effects 0.000 description 1
230000011278 mitosis Effects 0.000 description 1
229960005181 morphine Drugs 0.000 description 1
230000004899 motility Effects 0.000 description 1
230000036457 multidrug resistance Effects 0.000 description 1
201000006417 multiple sclerosis Diseases 0.000 description 1
230000035772 mutation Effects 0.000 description 1
YOHYSYJDKVYCJI-UHFFFAOYSA-N n-[3-[[6-[3-(trifluoromethyl)anilino]pyrimidin-4-yl]amino]phenyl]cyclopropanecarboxamide Chemical compound FC(F)(F)C1=CC=CC(NC=2N=CN=C(NC=3C=C(NC(=O)C4CC4)C=CC=3)C=2)=C1 YOHYSYJDKVYCJI-UHFFFAOYSA-N 0.000 description 1
KVBGVZZKJNLNJU-UHFFFAOYSA-N naphthalene-2-sulfonic acid Chemical compound C1=CC=CC2=CC(S(=O)(=O)O)=CC=C21 KVBGVZZKJNLNJU-UHFFFAOYSA-N 0.000 description 1
125000001624 naphthyl group Chemical group 0.000 description 1
239000002858 neurotransmitter agent Substances 0.000 description 1
229910017604 nitric acid Inorganic materials 0.000 description 1
125000004971 nitroalkyl group Chemical group 0.000 description 1
PLXPTFQGYWXIEA-UHFFFAOYSA-N nitroformonitrile Chemical compound [O-][N+](=O)C#N PLXPTFQGYWXIEA-UHFFFAOYSA-N 0.000 description 1
150000002829 nitrogen Chemical group 0.000 description 1
125000006574 non-aromatic ring group Chemical group 0.000 description 1
231100000252 nontoxic Toxicity 0.000 description 1
230000003000 nontoxic effect Effects 0.000 description 1
108020004707 nucleic acids Proteins 0.000 description 1
102000039446 nucleic acids Human genes 0.000 description 1
150000007523 nucleic acids Chemical class 0.000 description 1
235000016709 nutrition Nutrition 0.000 description 1
NIHNNTQXNPWCJQ-UHFFFAOYSA-N o-biphenylenemethane Natural products C1=CC=C2CC3=CC=CC=C3C2=C1 NIHNNTQXNPWCJQ-UHFFFAOYSA-N 0.000 description 1
QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
238000011275 oncology therapy Methods 0.000 description 1
230000003287 optical effect Effects 0.000 description 1
150000007524 organic acids Chemical class 0.000 description 1
229960003104 ornithine Drugs 0.000 description 1
150000003891 oxalate salts Chemical class 0.000 description 1
JMANVNJQNLATNU-UHFFFAOYSA-N oxalonitrile Chemical group N#CC#N JMANVNJQNLATNU-UHFFFAOYSA-N 0.000 description 1
125000005702 oxyalkylene group Chemical group 0.000 description 1
125000006503 p-nitrobenzyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1[N+]([O-])=O)C([H])([H])* 0.000 description 1
FJKROLUGYXJWQN-UHFFFAOYSA-N papa-hydroxy-benzoic acid Natural products OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 description 1
238000005192 partition Methods 0.000 description 1
230000007310 pathophysiology Effects 0.000 description 1
230000037361 pathway Effects 0.000 description 1
125000004817 pentamethylene group Chemical group [H]C([H])([*:2])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[*:1] 0.000 description 1
125000002255 pentenyl group Chemical group C(=CCCC)* 0.000 description 1
150000002978 peroxides Chemical class 0.000 description 1
239000008177 pharmaceutical agent Substances 0.000 description 1
230000000144 pharmacologic effect Effects 0.000 description 1
125000005561 phenanthryl group Chemical group 0.000 description 1
COLNVLDHVKWLRT-UHFFFAOYSA-N phenylalanine Natural products OC(=O)C(N)CC1=CC=CC=C1 COLNVLDHVKWLRT-UHFFFAOYSA-N 0.000 description 1
125000002467 phosphate group Chemical group [H]OP(=O)(O[H])O[*] 0.000 description 1
229910052698 phosphorus Inorganic materials 0.000 description 1
239000011574 phosphorus Substances 0.000 description 1
230000035479 physiological effects, processes and functions Effects 0.000 description 1
IUGYQRQAERSCNH-UHFFFAOYSA-N pivalic acid Chemical compound CC(C)(C)C(O)=O IUGYQRQAERSCNH-UHFFFAOYSA-N 0.000 description 1
WSHYKIAQCMIPTB-UHFFFAOYSA-M potassium;2-oxo-3-(3-oxo-1-phenylbutyl)chromen-4-olate Chemical compound [K+].[O-]C=1C2=CC=CC=C2OC(=O)C=1C(CC(=O)C)C1=CC=CC=C1 WSHYKIAQCMIPTB-UHFFFAOYSA-M 0.000 description 1
238000002360 preparation method Methods 0.000 description 1
102000004196 processed proteins & peptides Human genes 0.000 description 1
238000012545 processing Methods 0.000 description 1
235000019260 propionic acid Nutrition 0.000 description 1
125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
MWWATHDPGQKSAR-UHFFFAOYSA-N propyne Chemical group CC#C MWWATHDPGQKSAR-UHFFFAOYSA-N 0.000 description 1
230000004224 protection Effects 0.000 description 1
239000003909 protein kinase inhibitor Substances 0.000 description 1
108010067366 proto-oncogene protein c-fes-fps Proteins 0.000 description 1
UBQKCCHYAOITMY-UHFFFAOYSA-N pyridin-2-ol Chemical compound OC1=CC=CC=N1 UBQKCCHYAOITMY-UHFFFAOYSA-N 0.000 description 1
VUVGMQNYJPPCCC-UHFFFAOYSA-N pyrido[1,2-a]indole Chemical compound C1=CC=CC2=CC3=CC=CC=C3N21 VUVGMQNYJPPCCC-UHFFFAOYSA-N 0.000 description 1
JBDKAABFESSFMV-UHFFFAOYSA-N pyrrolo[1,2-a]pyrimidine Chemical compound N1=CC=CN2C=CC=C21 JBDKAABFESSFMV-UHFFFAOYSA-N 0.000 description 1
RIEKLTCRUGDAPM-UHFFFAOYSA-N pyrrolo[1,2-c]pyrimidine Chemical compound C1=CN=CN2C=CC=C21 RIEKLTCRUGDAPM-UHFFFAOYSA-N 0.000 description 1
229940107700 pyruvic acid Drugs 0.000 description 1
IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 1
230000005855 radiation Effects 0.000 description 1
150000003254 radicals Chemical class 0.000 description 1
108700042226 ras Genes Proteins 0.000 description 1
238000004064 recycling Methods 0.000 description 1
230000009467 reduction Effects 0.000 description 1
238000006722 reduction reaction Methods 0.000 description 1
230000004044 response Effects 0.000 description 1
229910052707 ruthenium Inorganic materials 0.000 description 1
229960004889 salicylic acid Drugs 0.000 description 1
150000003902 salicylic acid esters Chemical class 0.000 description 1
UQDJGEHQDNVPGU-UHFFFAOYSA-N serine phosphoethanolamine Chemical compound [NH3+]CCOP([O-])(=O)OCC([NH3+])C([O-])=O UQDJGEHQDNVPGU-UHFFFAOYSA-N 0.000 description 1
230000011664 signaling Effects 0.000 description 1
230000009131 signaling function Effects 0.000 description 1
229910000029 sodium carbonate Inorganic materials 0.000 description 1
241000894007 species Species 0.000 description 1
239000008117 stearic acid Substances 0.000 description 1
238000007920 subcutaneous administration Methods 0.000 description 1
125000005346 substituted cycloalkyl group Chemical group 0.000 description 1
238000006467 substitution reaction Methods 0.000 description 1
239000000758 substrate Substances 0.000 description 1
150000003890 succinate salts Chemical class 0.000 description 1
150000003871 sulfonates Chemical class 0.000 description 1
150000003460 sulfonic acids Chemical class 0.000 description 1
239000011975 tartaric acid Substances 0.000 description 1
235000002906 tartaric acid Nutrition 0.000 description 1
229940095064 tartrate Drugs 0.000 description 1
150000003892 tartrate salts Chemical class 0.000 description 1
WMOVHXAZOJBABW-UHFFFAOYSA-N tert-butyl acetate Chemical compound CC(=O)OC(C)(C)C WMOVHXAZOJBABW-UHFFFAOYSA-N 0.000 description 1
125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
125000003718 tetrahydrofuranyl group Chemical group 0.000 description 1
125000001412 tetrahydropyranyl group Chemical group 0.000 description 1
125000003554 tetrahydropyrrolyl group Chemical group 0.000 description 1
125000003698 tetramethyl group Chemical group [H]C([H])([H])* 0.000 description 1
150000003536 tetrazoles Chemical class 0.000 description 1
SMZMHUCIDGHERP-UHFFFAOYSA-N thieno[2,3-b]pyridine Chemical compound C1=CN=C2SC=CC2=C1 SMZMHUCIDGHERP-UHFFFAOYSA-N 0.000 description 1
GDQBPBMIAFIRIU-UHFFFAOYSA-N thieno[2,3-c]pyridine Chemical compound C1=NC=C2SC=CC2=C1 GDQBPBMIAFIRIU-UHFFFAOYSA-N 0.000 description 1
DBDCNCCRPKTRSD-UHFFFAOYSA-N thieno[3,2-b]pyridine Chemical compound C1=CC=C2SC=CC2=N1 DBDCNCCRPKTRSD-UHFFFAOYSA-N 0.000 description 1
125000005297 thienyloxy group Chemical group S1C(=CC=C1)O* 0.000 description 1
150000007970 thio esters Chemical class 0.000 description 1
125000005323 thioketone group Chemical group 0.000 description 1
125000004055 thiomethyl group Chemical group [H]SC([H])([H])* 0.000 description 1
229930192474 thiophene Natural products 0.000 description 1
210000001519 tissue Anatomy 0.000 description 1
238000013518 transcription Methods 0.000 description 1
230000035897 transcription Effects 0.000 description 1
230000014616 translation Effects 0.000 description 1
238000013519 translation Methods 0.000 description 1
150000003852 triazoles Chemical class 0.000 description 1
LENLQGBLVGGAMF-UHFFFAOYSA-N tributyl([1,2,4]triazolo[1,5-a]pyridin-6-yl)stannane Chemical compound C1=C([Sn](CCCC)(CCCC)CCCC)C=CC2=NC=NN21 LENLQGBLVGGAMF-UHFFFAOYSA-N 0.000 description 1
IMFACGCPASFAPR-UHFFFAOYSA-N tributylamine Chemical compound CCCCN(CCCC)CCCC IMFACGCPASFAPR-UHFFFAOYSA-N 0.000 description 1
125000003258 trimethylene group Chemical group [H]C([H])([*:2])C([H])([H])C([H])([H])[*:1] 0.000 description 1
125000002221 trityl group Chemical group [H]C1=C([H])C([H])=C([H])C([H])=C1C([*])(C1=C(C(=C(C(=C1[H])[H])[H])[H])[H])C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 1
229960004418 trolamine Drugs 0.000 description 1
OUYCCCASQSFEME-UHFFFAOYSA-N tyrosine Natural products OC(=O)C(N)CC1=CC=C(O)C=C1 OUYCCCASQSFEME-UHFFFAOYSA-N 0.000 description 1
PXXNTAGJWPJAGM-UHFFFAOYSA-N vertaline Natural products C1C2C=3C=C(OC)C(OC)=CC=3OC(C=C3)=CC=C3CCC(=O)OC1CC1N2CCCC1 PXXNTAGJWPJAGM-UHFFFAOYSA-N 0.000 description 1
229920002554 vinyl polymer Polymers 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/04—Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P13/00—Drugs for disorders of the urinary system
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P13/00—Drugs for disorders of the urinary system
- A61P13/12—Drugs for disorders of the urinary system of the kidneys
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
- A61P17/02—Drugs for dermatological disorders for treating wounds, ulcers, burns, scars, keloids, or the like
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
- A61P17/06—Antipsoriatics
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
- A61P17/14—Drugs for dermatological disorders for baldness or alopecia
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
- A61P17/16—Emollients or protectives, e.g. against radiation
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
- A61P19/02—Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
- A61P19/08—Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/14—Drugs for disorders of the nervous system for treating abnormal movements, e.g. chorea, dyskinesia
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
- A61P35/02—Antineoplastic agents specific for leukemia
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/02—Immunomodulators
- A61P37/06—Immunosuppressants, e.g. drugs for graft rejection
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/08—Antiallergic agents
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/12—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains three hetero rings
- C07D487/14—Ortho-condensed systems
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D519/00—Heterocyclic compounds containing more than one system of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring system not provided for in groups C07D453/00 or C07D455/00

Landscapes

Health & Medical Sciences (AREA)
Organic Chemistry (AREA)
Chemical & Material Sciences (AREA)
Medicinal Chemistry (AREA)
General Health & Medical Sciences (AREA)
Veterinary Medicine (AREA)
Public Health (AREA)
Animal Behavior & Ethology (AREA)
Chemical Kinetics & Catalysis (AREA)
General Chemical & Material Sciences (AREA)
Life Sciences & Earth Sciences (AREA)
Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
Pharmacology & Pharmacy (AREA)
Engineering & Computer Science (AREA)
Bioinformatics & Cheminformatics (AREA)
Immunology (AREA)
Dermatology (AREA)
Biomedical Technology (AREA)
Neurosurgery (AREA)
Physical Education & Sports Medicine (AREA)
Neurology (AREA)
Rheumatology (AREA)
Urology & Nephrology (AREA)
Oncology (AREA)
Orthopedic Medicine & Surgery (AREA)
Heart & Thoracic Surgery (AREA)
Pulmonology (AREA)
Cardiology (AREA)
Psychology (AREA)
Toxicology (AREA)
Communicable Diseases (AREA)
Hematology (AREA)
Psychiatry (AREA)
Vascular Medicine (AREA)
Transplantation (AREA)
Pain & Pain Management (AREA)
Hospice & Palliative Care (AREA)
Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Nitrogen Condensed Heterocyclic Rings (AREA)
Nitrogen- Or Sulfur-Containing Heterocyclic Ring Compounds With Rings Of Six Or More Members (AREA)

TW097137049A 2007-09-25 2008-09-25 類Ｐｏｌｏ激酶抑制劑 TWI436769B (zh)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
US97512707P	2007-09-25	2007-09-25
US3730308P	2008-03-17	2008-03-17

Publications (2)

Publication Number	Publication Date
TW200927135A TW200927135A (en)	2009-07-01
TWI436769B true TWI436769B (zh)	2014-05-11

Family

ID=40219644

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
TW097137049A TWI436769B (zh)	2007-09-25	2008-09-25	類Ｐｏｌｏ激酶抑制劑

Country Status (26)

Country	Link
US (4)	US20110201818A1 (es)
EP (3)	EP2564850B1 (es)
JP (2)	JP5372939B2 (es)
KR (2)	KR101444924B1 (es)
CN (2)	CN103122001A (es)
AR (1)	AR071729A1 (es)
AU (1)	AU2008304417B2 (es)
BR (1)	BRPI0817315A2 (es)
CA (2)	CA2699607A1 (es)
CL (1)	CL2008002852A1 (es)
CO (1)	CO6270231A2 (es)
CR (1)	CR11370A (es)
DO (1)	DOP2010000091A (es)
EA (1)	EA019487B1 (es)
EC (1)	ECSP10010129A (es)
ES (1)	ES2488966T3 (es)
GE (1)	GEP20125704B (es)
MA (1)	MA31763B1 (es)
MX (2)	MX2010003249A (es)
MY (1)	MY152283A (es)
NZ (1)	NZ584760A (es)
PE (1)	PE20090710A1 (es)
TN (1)	TN2010000131A1 (es)
TW (1)	TWI436769B (es)
WO (2)	WO2009042711A1 (es)
ZA (1)	ZA201002543B (es)

Families Citing this family (38)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US7622463B2 (en)	2006-02-14	2009-11-24	Vertex Pharmaceuticals Incorporated	Dihydrodiazepines useful as inhibitors of protein kinases
EP2564850B1 (en) *	2007-09-25	2014-08-13	Takeda Pharmaceutical Company Limited	Polo-like kinase inhibitors
EP2610256B1 (en) *	2007-09-28	2016-04-27	Cyclacel Limited	Pyrimidine derivatives as protein kinase inhibitors
WO2009153197A1 (en) *	2008-06-18	2009-12-23	F. Hoffmann-La Roche Ag	Halo-substituted pyrimidodiazepines as plkl inhibitors
AU2010232644A1 (en) *	2009-03-31	2011-10-20	Arqule, Inc.	Substituted tetrahydropyrazolo-pyrido-azepin compounds
CA2756568C (en)	2009-04-06	2018-02-13	University Health Network	Kinase inhibitors and method of treating cancer with same
ES2567280T3 (es)	2009-09-25	2016-04-21	Vertex Pharmaceuticals Incorporated	Métodos para preparar derivados de pirimidina útiles como inhibidores de proteína quinasa
EP2480553A2 (en) *	2009-09-25	2012-08-01	Vertex Pharmaceuticals Incorporated	Methods for preparing pyrimidine derivatives useful as protein kinase inhibitors
EP2516441B1 (en)	2009-12-23	2015-01-21	Elan Pharmaceuticals Inc.	Pteridinones as inhibitors of polo-like kinase
ES2639757T3 (es)	2010-04-06	2017-10-30	University Health Network	Síntesis de 2-(1H-indazol-6-il)espiro[ciclopropan-1,3'-indolin]-2'-onas quirales
TW201307347A (zh)	2010-11-01	2013-02-16	Arqule Inc	經取代苯並－咪唑並－吡啶並－二氮呯化合物
US9006477B2 (en) *	2011-07-07	2015-04-14	Ihara Chemical Industry Co., Ltd.	Method for producing nitrobenzene compound
WO2013058344A1 (ja) *	2011-10-21	2013-04-25	武田薬品工業株式会社	Plk1阻害剤の効果を予測する方法
EA031569B1 (ru)	2013-10-18	2019-01-31	Юниверсити Хелс Нетуорк	Солевые и кристаллические формы ингибитора plk-4
CN106029653A (zh)	2014-01-31	2016-10-12	达纳-法伯癌症研究所股份有限公司	二氨基嘧啶苯砜衍生物及其用途
WO2015117087A1 (en)	2014-01-31	2015-08-06	Dana-Farber Cancer Institute, Inc.	Uses of diazepane derivatives
BR112017002369A2 (pt)	2014-08-08	2017-12-05	Dana Farber Cancer Inst Inc	derivados de diazepana e usos dos mesmos
EP3307728A4 (en)	2015-06-12	2019-07-17	Dana Farber Cancer Institute, Inc.	COMBINATION THERAPY OF TRANSCRIPTION INHIBITORS AND CHINESE INHIBITORS
RU2750164C2 (ru)	2015-09-11	2021-06-22	Дана-Фарбер Кэнсер Инститьют, Инк.	Цианотиенотриазолодиазепины и пути их применения
PE20181086A1 (es)	2015-09-11	2018-07-05	Dana Farber Cancer Inst Inc	Acetamida tienotrizolodiazepinas y usos de las mismas
MX2018006499A (es)	2015-11-25	2018-08-01	Dana Farber Cancer Inst Inc	Inhibidores de bromodominio bivalentes y usos de los mismos.
TW202506629A (zh) *	2016-05-05	2025-02-16	美商嘉來克生命科學有限責任公司	整合應激途徑之調節劑
AU2020264143A1 (en)	2019-04-24	2021-10-28	University Health Network	Crystal form S4 of the PLK4 inhibitor (1R,2S)-(E)-2-(3-(4-((cis-2,6-dimethylmorpholino)methyl)styryl)- 1 H-imidazol-6- yl)-5'-methoxyspiro(cyclopropane-1,3'-indolin)-2'-one fumarate
WO2021194319A1 (en)	2020-03-27	2021-09-30	Uppthera	Vanillin derivative compounds inducing selective degradation of plk1
WO2022145989A1 (ko) *	2020-12-31	2022-07-07	(주) 업테라	선택적 plk1 억제제로서의 피리미도디아제핀 유도체
CN116761806B (zh) *	2021-02-08	2025-10-10	上海复星医药产业发展有限公司	5，6-二氢噻吩并[3，4-h]喹唑啉类化合物
WO2024229406A1 (en)	2023-05-04	2024-11-07	Revolution Medicines, Inc.	Combination therapy for a ras related disease or disorder
WO2025034702A1 (en)	2023-08-07	2025-02-13	Revolution Medicines, Inc.	Rmc-6291 for use in the treatment of ras protein-related disease or disorder
TW202530228A (zh)	2023-10-12	2025-08-01	美商銳新醫藥公司	Ｒａｓ抑制劑
WO2025171296A1 (en)	2024-02-09	2025-08-14	Revolution Medicines, Inc.	Ras inhibitors
WO2025240847A1 (en)	2024-05-17	2025-11-20	Revolution Medicines, Inc.	Ras inhibitors
US20250375445A1 (en)	2024-06-07	2025-12-11	Revolution Medicines, Inc.	Methods of treating a ras protein-related disease or disorder
WO2025265060A1 (en)	2024-06-21	2025-12-26	Revolution Medicines, Inc.	Therapeutic compositions and methods for managing treatment-related effects
WO2026006747A1 (en)	2024-06-28	2026-01-02	Revolution Medicines, Inc.	Ras inhibitors
WO2026015796A1 (en)	2024-07-12	2026-01-15	Revolution Medicines, Inc.	Methods of treating a ras related disease or disorder
WO2026015790A1 (en)	2024-07-12	2026-01-15	Revolution Medicines, Inc.	Methods of treating a ras related disease or disorder
WO2026015801A1 (en)	2024-07-12	2026-01-15	Revolution Medicines, Inc.	Methods of treating a ras related disease or disorder
WO2026015825A1 (en)	2024-07-12	2026-01-15	Revolution Medicines, Inc.	Use of ras inhibitor for treating pancreatic cancer

Family Cites Families (25)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US3710795A (en)	1970-09-29	1973-01-16	Alza Corp	Drug-delivery device with stretched, rate-controlling membrane
US4044126A (en)	1972-04-20	1977-08-23	Allen & Hanburys Limited	Steroidal aerosol compositions and process for the preparation thereof
GB1429184A (en)	1972-04-20	1976-03-24	Allen & Hanburys Ltd	Physically anti-inflammatory steroids for use in aerosols
USRE28819E (en)	1972-12-08	1976-05-18	Syntex (U.S.A.) Inc.	Dialkylated glycol compositions and medicament preparations containing same
US4410545A (en)	1981-02-13	1983-10-18	Syntex (U.S.A.) Inc.	Carbonate diester solutions of PGE-type compounds
US4328245A (en)	1981-02-13	1982-05-04	Syntex (U.S.A.) Inc.	Carbonate diester solutions of PGE-type compounds
US4358603A (en)	1981-04-16	1982-11-09	Syntex (U.S.A.) Inc.	Acetal stabilized prostaglandin compositions
US4409239A (en)	1982-01-21	1983-10-11	Syntex (U.S.A.) Inc.	Propylene glycol diester solutions of PGE-type compounds
WO2001019825A1 (en)	1999-09-15	2001-03-22	Warner-Lambert Company	Pteridinones as kinase inhibitors
MXPA02002938A (es)	1999-09-17	2004-12-06	Abbott Gmbh & Co Kg	Inhibidores de cinasa como agentes agentes terapeuticos.
US6806272B2 (en)	2001-09-04	2004-10-19	Boehringer Ingelheim Pharma Kg	Dihydropteridinones, processes for preparing them and their use as pharmaceutical compositions
HRP20040213A2 (en)	2001-09-04	2005-02-28	Boehringer Ingelheim Pharma Gmbh & Co.Kg	Novel dihydropteridinones, method for producing the same and the use thereof as medicaments
US6861422B2 (en)	2003-02-26	2005-03-01	Boehringer Ingelheim Pharma Gmbh & Co. Kg	Dihydropteridinones, processes for preparing them and their use as pharmaceutical compositions
US20060074088A1 (en)	2004-08-14	2006-04-06	Boehringer Ingelheim International Gmbh	Dihydropteridinones for the treatment of cancer diseases
EP1632493A1 (de)	2004-08-25	2006-03-08	Boehringer Ingelheim Pharma GmbH & Co.KG	Dihydropteridinonderivative, Verfahren zu deren Herstellung und deren Verwendung als Arzneimittel
EP1630163A1 (de)	2004-08-25	2006-03-01	Boehringer Ingelheim Pharma GmbH & Co.KG	Dihydropteridinonderivative, Verfahren zu deren Herstellung und deren Verwendung als Arzneimittel
EP1784406A1 (de)	2004-08-27	2007-05-16	Boehringer Ingelheim International GmbH	Dihydropteridinone, verfahren zu deren herstellung und deren verwendung als arzneimittel
US7622463B2 (en)	2006-02-14	2009-11-24	Vertex Pharmaceuticals Incorporated	Dihydrodiazepines useful as inhibitors of protein kinases
JP2009537500A (ja)	2006-05-19	2009-10-29	アストラゼネカアクチボラグ	増殖抑制剤としてのジヒドロプテリジン化合物
TW200808325A (en)	2006-07-06	2008-02-16	Astrazeneca Ab	Novel compounds
EP2139892B1 (en) *	2007-03-22	2011-09-14	Takeda Pharmaceutical Company Limited	Substituted pyrimidodiazepines useful as plk1 inhibitors
AU2008287339A1 (en)	2007-08-15	2009-02-19	Vertex Pharmaceuticals Incorporated	4-(9-(3, 3-difluorocyclopentyl) -5, 7, 7-trimethyl-6-oxo-6, 7, 8, 9-tetrahydro-5H-pyrimido [4, 5-b][1, 4] diazepin-2-ylamino)-3-methoxybenzamide Derivatives as Inhibitors of the Human Protein Kinases PLK1 to PLK4 for the Treatment of Proliferative Diseases
EP2564850B1 (en) *	2007-09-25	2014-08-13	Takeda Pharmaceutical Company Limited	Polo-like kinase inhibitors
EP2610256B1 (en)	2007-09-28	2016-04-27	Cyclacel Limited	Pyrimidine derivatives as protein kinase inhibitors
WO2009153197A1 (en)	2008-06-18	2009-12-23	F. Hoffmann-La Roche Ag	Halo-substituted pyrimidodiazepines as plkl inhibitors

2008
- 2008-09-24 EP EP12189293.9A patent/EP2564850B1/en active Active
- 2008-09-24 ES ES08834219.1T patent/ES2488966T3/es active Active
- 2008-09-24 CA CA2699607A patent/CA2699607A1/en not_active Abandoned
- 2008-09-24 MX MX2010003249A patent/MX2010003249A/es active IP Right Grant
- 2008-09-24 WO PCT/US2008/077558 patent/WO2009042711A1/en not_active Ceased
- 2008-09-24 CN CN2012105686507A patent/CN103122001A/zh active Pending
- 2008-09-24 CN CN2008801169537A patent/CN101917995A/zh active Pending
- 2008-09-24 EA EA201070395A patent/EA019487B1/ru not_active IP Right Cessation
- 2008-09-24 AU AU2008304417A patent/AU2008304417B2/en not_active Ceased
- 2008-09-24 KR KR1020107009029A patent/KR101444924B1/ko not_active Expired - Fee Related
- 2008-09-24 US US12/680,183 patent/US20110201818A1/en not_active Abandoned
- 2008-09-24 MY MYPI20101261 patent/MY152283A/en unknown
- 2008-09-24 JP JP2010526067A patent/JP5372939B2/ja not_active Expired - Fee Related
- 2008-09-24 EP EP08834219.1A patent/EP2205241B1/en active Active
- 2008-09-24 BR BRPI0817315 patent/BRPI0817315A2/pt not_active IP Right Cessation
- 2008-09-24 NZ NZ584760A patent/NZ584760A/en not_active IP Right Cessation
- 2008-09-24 US US12/237,306 patent/US8026234B2/en not_active Expired - Fee Related
- 2008-09-24 KR KR1020147017278A patent/KR20140097440A/ko not_active Ceased
- 2008-09-24 GE GEAP200811771A patent/GEP20125704B/en unknown
- 2008-09-25 PE PE2008001672A patent/PE20090710A1/es not_active Application Discontinuation
- 2008-09-25 US US12/680,142 patent/US8202990B2/en not_active Expired - Fee Related
- 2008-09-25 CA CA2700295A patent/CA2700295A1/en not_active Abandoned
- 2008-09-25 WO PCT/US2008/077746 patent/WO2009042806A1/en not_active Ceased
- 2008-09-25 EP EP08833760A patent/EP2197442B1/en not_active Not-in-force
- 2008-09-25 AR ARP080104179A patent/AR071729A1/es unknown
- 2008-09-25 MX MX2010003244A patent/MX2010003244A/es active IP Right Grant
- 2008-09-25 CL CL2008002852A patent/CL2008002852A1/es unknown
- 2008-09-25 TW TW097137049A patent/TWI436769B/zh not_active IP Right Cessation
- 2008-09-25 JP JP2010526073A patent/JP2010540464A/ja active Pending
2010
- 2010-03-22 TN TNP2010000131A patent/TN2010000131A1/fr unknown
- 2010-03-25 DO DO2010000091A patent/DOP2010000091A/es unknown
- 2010-04-08 MA MA32753A patent/MA31763B1/fr unknown
- 2010-04-09 CO CO10041197A patent/CO6270231A2/es active IP Right Grant
- 2010-04-12 ZA ZA2010/02543A patent/ZA201002543B/en unknown
- 2010-04-14 CR CR11370A patent/CR11370A/es unknown
- 2010-04-23 EC EC2010010129A patent/ECSP10010129A/es unknown
- 2010-12-07 US US12/962,557 patent/US8318727B2/en not_active Expired - Fee Related

Also Published As

Publication number	Publication date
TW200927135A (en)	2009-07-01
JP2010540463A (ja)	2010-12-24
HK1145144A1 (en)	2011-04-08
US20110082111A1 (en)	2011-04-07
AU2008304417B2 (en)	2013-07-18
CN103122001A (zh)	2013-05-29
TN2010000131A1 (en)	2011-09-26
WO2009042711A4 (en)	2009-06-04
ECSP10010129A (es)	2010-06-29
US8318727B2 (en)	2012-11-27
JP5372939B2 (ja)	2013-12-18
NZ584760A (en)	2012-03-30
EP2197442B1 (en)	2012-09-12
BRPI0817315A2 (pt)	2015-03-17
US20090281092A1 (en)	2009-11-12
KR20140097440A (ko)	2014-08-06
CO6270231A2 (es)	2011-04-20
MX2010003244A (es)	2010-04-21
EA201070395A1 (ru)	2010-10-29
EA019487B1 (ru)	2014-04-30
US8026234B2 (en)	2011-09-27
KR101444924B1 (ko)	2014-10-07
EP2564850B1 (en)	2014-08-13
EP2564850A1 (en)	2013-03-06
PE20090710A1 (es)	2009-07-15
AU2008304417A1 (en)	2009-04-02
EP2205241B1 (en)	2014-05-21
EP2197442A1 (en)	2010-06-23
CA2700295A1 (en)	2009-04-02
KR20100087292A (ko)	2010-08-04
GEP20125704B (en)	2012-12-10
ZA201002543B (en)	2011-11-30
AR071729A1 (es)	2010-07-14
DOP2010000091A (es)	2010-07-31
MA31763B1 (fr)	2010-10-01
US8202990B2 (en)	2012-06-19
WO2009042711A1 (en)	2009-04-02
MY152283A (en)	2014-09-15
WO2009042806A1 (en)	2009-04-02
CN101917995A (zh)	2010-12-15
MX2010003249A (es)	2010-11-09
CR11370A (es)	2010-07-16
US20100222575A1 (en)	2010-09-02
EP2205241A1 (en)	2010-07-14
US20110201818A1 (en)	2011-08-18
CL2008002852A1 (es)	2009-03-27
CA2699607A1 (en)	2009-04-02
JP2010540464A (ja)	2010-12-24
ES2488966T3 (es)	2014-09-01

Publication	Publication Date	Title
TWI436769B (zh)	2014-05-11	類Ｐｏｌｏ激酶抑制劑
EP3768664B1 (en)	2024-09-04	Pyrazinone derivatives as shp2 inhibitors and uses thereof
US20090291938A1 (en)	2009-11-26	Polo-like kinase inhibitors
KR102030609B1 (ko)	2019-10-11	Ｐｉ３ｋ 억제제로서 헤테로시클릴아민
JP2009532375A (ja)	2009-09-10	キナーゼ阻害剤
JP2009511503A (ja)	2009-03-19	キナーゼ阻害剤
JP2010505961A (ja)	2010-02-25	キナーゼ阻害剤
EP2145877A2 (en)	2010-01-20	Aurora Kinase inhibitors
US20090312288A1 (en)	2009-12-17	Kinase inhibitors
US8278450B2 (en)	2012-10-02	Kinase inhibitors
HK1145144B (en)	2014-08-29	Polo-like kinase inhibitors
HK1139947A (en)	2010-09-30	Aurora kinase inhibitors
CN101573335A (zh)	2009-11-04	激酶抑制剂

Legal Events

Date	Code	Title	Description
2016-02-11	MM4A	Annulment or lapse of patent due to non-payment of fees